Final CVD Prevention Report 08 Oct 18
Final CVD Prevention Report 08 Oct 18
October 2018
Report and case studies
This publication has been based on information and data provided by a number of third
parties. While care was taken in the preparation of the information in this report and every
effort has been made to ensure the information is accurate and up-to-date, SPH accepts no
responsibility for gaps or limitations in the information.
Acknowledgements
With acknowledgment and thanks to all those who provided information or material and who
participated in interviews.
Contents
6 Discussion ..................................................................................... 42
Whole population approach to raising awareness and changing lifestyle ..................... 42
Detection of people with high risk of CVD .................................................................... 43
Prevention for people at high risk of a first or subsequent CVD event or diagnosis. ..... 45
7 Conclusion ..................................................................................... 46
8 Appendices .................................................................................... 48
Appendix 1: Framework for information gathered for CVD prevention case studies from
interviews and programme documentation ................................................................. 48
Appendix 2: Socio ecological model and the influencers on health status with examples
of policy, strategy, guidance and media campaigns used in England to promote CVD
prevention .................................................................................................................. 50
Appendix 3: Australia COACH Programme ................................................................ 58
Appendix 4: Finland DEHKO And One Life................................................................. 69
Appendix 5: France ESCAPE Trial ............................................................................. 79
Appendix 6: Netherlands Vascular Risk ...................................................................... 88
Appendix 7: Canada CHAP Program.......................................................................... 96
Appendix 8: Healthy Japan 21 .................................................................................. 106
Appendix 9: Franklin County CVD Risk Reduction ................................................... 115
Appendix 10: USA HONU Project ............................................................................. 123
Appendix 11: Hypertension Canada ......................................................................... 133
Appendix 12: Hypertension Canada ......................................................................... 143
Solutions for Public Health (SPH) was commissioned by the British Heart Foundation (BHF)
and Public Health England (PHE) to identify and describe cardiovascular disease prevention
programmes successfully implemented in countries outside the UK. SPH developed case
studies for 10 of these programmes that illustrate approaches that may be applicable and
effective within the UK. This report sets out how SPH undertook this project, the current
context in England and the case studies that emerged from the information gathering
process.
The programmes identified that were developed into case studies were a mix of prevention
approaches, some were single interventions and others were programmes with multiple
initiatives. They were all multifaceted in that they targeted a range of modifiable CVD risk
factors including those that would benefit from lifestyle change and/or optimisation of
medical management. Some programmes also described in detail how people with
undetected high risk of CVD were identified.
Four of the case studies focus on people with CVD or a high risk of CVD, with risk factors
such as, atrial fibrillation, hypertension, hypercholesterolaemia and diabetes. Those with
current CVD or a high risk of CVD are offered interventions to reduce their risk with the aim
of averting further morbidity and impact on health services. A further four case studies are
programmes with a combination of prevention approaches encompassing both prevention of
developing, and amelioration of, CVD risk factors across populations. These programmes
typically comprise multiple small initiatives under one programme umbrella.
Two cases studies are national initiatives with a core aim to improve the detection and
effective management of people at risk of CVD. This is achieved through building research
capacity, collaborating with stakeholders, education of public and professionals, developing
guidelines and promoting evidence based activities in health services and the community.
The COACH Program® (Coaching patients On Achieving Cardiovascular Health) focuses on increasing the engagement of individuals in understanding and
improving their own health by understanding how lifestyle impacts on CVD risk and identifying any treatment gaps in the management of conditions. The
intervention consists of coaching sessions for patients by trained nurses by phone over a minimum of three sessions.
Outcomes
DEHKO was launched in Finland as part of the Finnish National Diabetes Programme (FIN D2D), from 2000 to 2010 and aimed to improve self care and
prevent and reduce complications from type 2 diabetes. From 2011, the DEHKO programme expanded to include raising awareness and reducing risk of non
communicable diseases with common risk factors including cardiovascular disease (CVD), dementia, chronic obstructive pulmonary disease (COPD) and
type 2 diabetes. This included using a brief screening tool followed by an in depth health check up and education/motivational individual and group sessions
for those at high risk of CVD. ‘One Life’ is supported by a collaboration of the Finnish Diabetes, Brain and Heart Associations and focuses on supporting
people to make lifestyle changes to improve modifiable risk factors.
Outcomes
ESCAPE was designed to show whether a multifaceted intervention, aimed at general practitioners (GPs), could significantly increase the proportion of
hypertensive patients at high risk of cardiovascular disease (CVD) who achieved all their recommended therapeutic targets. This involved one day of GP
training and support to ensure patients were managed according to guidelines and followed up. A trial with an intervention group and no intervention group
measured the effect.
Outcomes
Comparisons at 2 years between intervention group and no intervention group Odds ratio (95% P value
confidence interval)
Patients achieving all their therapeutic targets compared with no intervention 1.89(1.09 to 3.27) p = 0.02
Patients achieving their blood pressure targets compared with no intervention 2.03(1.44 to 2.88) p < 0.0001
Difference in blood
pressure
Additional decrease in systolic blood pressure in intervention group compared with 4.8mmHg p < 0.0001
control
Additional decrease in diastolic blood pressures in intervention group compared with 1.9mmHg P<0.0001
control
This programme was designed to improve and add to standard nurse-led vascular risk factor management of patients with the addition of web based support
focused on lifestyle change and adherence to medication following a CVD event.
Outcomes
CHAP is a community based model of cardiovascular disease (CVD) prevention which has been used in a range of different communities. It encourages
people to become more aware of their cardiovascular risk and to acquire self-management skills. Increased detection of people at high risk of developing
CVD results in referral and the opportunity to manage the condition medically.
Outcomes
Longitudinal study of 13,596 people in 22 communities over 18 Baseline mean 18 months follow up
months
People attending ≥2 CHAP sessions improvement in blood pressure 142/78mmHg 123/69 mmHg
Rate ratio(95% CI) P value
Reduction in rate of acute myocardial infarctions 0.87(0.79 to 0.97) p=0.008
Reduction in congestive heart failure 0.90(0.81 to 0.99) p=0.029
No change in rate of stroke 0.99(0.88 to 1.12) p=0.89
No change in all cause mortality 0.98(0.92 to 1.03) p=0.38
No change in hospital death 0.86(0.73 to 1.01) p=0.06
Japan has embarked on a national health policy change to prevent lifestyle-related diseases, including cardiovascular disease (CVD) and diabetes. Following
the detection of high CVD risk (via the annual health check up) people are invited to participate in individual or group sessions to motivate them to reduce
their risk of metabolic syndrome and CVD.
Outcomes
Intervention No intervention P value
Waist circumference (WC) - clinically relevant (>5%) reduction - 21.4% 16.1% P<0.001
proportion(%) of participants at 3 years
BMI - clinically relevant(>5%) reduction - proportion(%) 17.6% 13.6% P<0.001
participants at 3 years
Reversal of metabolic syndrome – number of participants 47% 41.5% P<0.001
Reductions in systolic blood pressure (mmHg) -1.15mmHg -0.72mmHg
Reductions in diastolic BP -0.97mmHg -0.64mmHg
Odds ratio(95% confidence interval)
>5% reduction in WC intervention vs no intervention group 1.33(1.31 to 1.36) p<0.001
>5% reduction in BMI intervention vs no intervention n group 1.36(1.33 to 1.38) p<0.001
Reversal of metabolic syndrome 1.31(1.29 to 1.33) p<0.001
This programme was an integrated, community-wide comprehensive cardiovascular risk reduction programme started in 1970 with a 40-year follow-up
assessing the impact of risk factor improvements on reductions in morbidity and mortality. The initial focus was on hypertension detection and management
but over the years broadened to encompass other CVD risk factors.
Outcomes
Outcome
From 1994-2006 reduction in Franklin County’s hospitalisation rate Observed vs expected difference -17
discharges per 1,000 population
Reductions in total in and out of area hospital charges for Franklin County $5,450,362 (£3,919,300) per annum
residents per year due to drop in hospitalisation rate
From 1974/75 to 1977/8 increase in proportion of people with treated and Absolute increase of 24.7%
controlled hypertension
From 1986 to 2009 increase in the proportion of people with treated and Absolute increase of 28.5%
controlled cholesterol levels
Smoking quit rates (ever smokers who report they have quit) with Franklin Improved from 48.5% in 1994-5 to 69.5% in
County quit rates significantly higher than those seen in Maine and the US 2006-10
New Ulm is a small community of 17,000 people and local health organisations were keen to track the cardiovascular health of the population before and
during the implementation of community wide interventions. There were individual, family and organisational and community level interventions implemented
in order to influence behaviour and reduce modifiable cardiovascular disease (CVD) risk factors.
Outcomes
Measure 2008-9 2010-11 2012-13
Blood pressure at goal* 79.3% 82.3% 86.4%
On blood pressure medication* 41.8% 43.5% 44.0%
Low-density lipoprotein at goal* 68.9% 72.3% 71.1%
High-density lipoprotein at goal 63.8% 59.0% 58.0%
Cholesterol at goal* 59.2% 64.2% 64.1%
Triglycerides at goal* 66.3% 68.7% 70.2%
On lipid medication* 25.3% 27.7% 29.1%
Not obese 56.0% 55.5% 55.1%
ǂ
Fasting glucose at goal 46.9% 49.7% 48.2%
Smoking 11.3% 12.6% 13.6%
ASCVD 10-year risk score <7.5% 27.8% 28.9% 27.5%
Hypertension Canada was formed in 2010 from the merger of the Canadian Hypertension Society, the Canadian Hypertension Education Program and Blood
Pressure Canada. The main goal of this national initiative is to ensure that Canada is effective in controlling hypertension within the population. The core aim
of the programme is reducing misdiagnosis by ensuring that all healthcare professionals in Canada are appropriately trained to diagnose hypertension and
follow recommended guidance to mange the condition. In addition there is a focus on building research and surveillance capacity and coordinating the
networking of local and national stakeholders.
Outcomes
Measure 2007-09 2010-11 2012-13
Hypertension Prevalence (2020 target 13%) 19.6% 21.8% 22.6%
Awareness of condition (2020 target 95%) 83.4% 82.9% 84.3%
Diagnosed with hypertension with normal BP while not 8.5% 11.1% 6.6%
on antihypertensive drug treatment a (i.e. lifestyle
control of hypertension) (2020 target 40%)
Appropriate drug therapy (2020 target 87%) 79.9% 79.2% 79.6%
Blood pressure under control (2020 target 78%) 65.9% 64.1% 68.1%
In 2012 the Million Hearts initiative was established by the US Department of Health and Human Services, the Centre for Disease Control and Prevention
(CDC) and Centres for Medicare and Medicaid (CMS). This national initiative had a first phase, 5-year goal, of preventing 1 million cardiovascular events by
2017, and is now in its second phase, Million Hearts 2022. The core aim of the work is to align CVD prevention efforts across 50 states and 120 partners in
the US by focussing on implementation of the ABCS approach to CVD management (Aspirin when appropriate, Blood pressure control, Cholesterol
management, and Smoking cessation). Meaningful use of health tools and technology such as electronic records for identifying and monitoring patient groups
and introducing policies to eliminate artificial trans-fat intake, reduce tobacco use and reduce sodium intake are other key elements of the initiative.
Outcomes
Two programmes, Hypertension Canada and Million Hearts are national initiatives and foster
collaboration between health care providers and the implementation of evidence based
practice. Hypertension Canada focuses on research and the development of guidelines,
education of health care professionals to prioritise the accurate detection and management
of people with CVD risk. Million Hearts is a wide ranging national initiative with a small core
team who focus on promoting evidence based clinical quality improvement, detecting people
at risk of CVD using electronic health records, changing harmful behaviours such as
smoking, and high sodium and trans-fat intake. Organisations become partners in the Million
Hearts initiative and can secure funding though a variety of routes to support change in
practice. Both national programmes have not yet met their challenging targets but are slowly
progressing towards them using multiple approaches.
The case studies that developed a tried and tested sustainable approach that successfully
engaged relevant stakeholders that could be readily transferred to other communities whilst
reducing CVD risk, are arguably the most likely to be usefully adapted for use in England
and the wider UK. They were also the case studies that focused on long term sustainability
from the outset, and we suggest that this should be central to implementation of any
changes that follow from this work in the UK. The most successful three programmes
identified here from the evidence available (HONU, CHAP and COACH) all have a very
strong community focus although they are targeting different elements of prevention. They
are using schools, workplaces, community centres, pharmacies, or peoples own homes to
deliver the programme. HONU has the broadest approach drawing on all sectors of the
community, whilst CHAP has a more focused approach running community clinics to detect
CVD risk factors in the local population and COACH offers support in management of risk
factors by phone to people in their own homes. Going to where the people are, empowering
individuals and the wider community with information and an understanding of CVD risk, that
they can monitor themselves, is clearly important in the success of the programmes.
All three programmes built in mechanisms for ensuring that they were sustainable in the long
term with minimal continued investment which is a particularly important consideration, given
the constraints of resources at the current time. Strong leadership and governance of the
programmes was built into the mainstream running of each service or community
programme to ensure it was fully integrated as part of the approach to prevention. This led to
good community engagement and mobilisation with the use of volunteers to support the
delivery of the programmes in the case of HONU and CHAP. COACH meanwhile used and
trained a wider professional group to contact people at home to support them to be actively
engaged in reducing their own risk factors by optimising medication and making lifestyle
changes.
2 Methods
This project was built on the outcomes of PHE’s work to identify current and past CVD
prevention programmes implemented in the UK and internationally. PHE identified these
programmes through a structured review of published and unpublished literature and
developed a spreadsheet of relevant programmes and their outcome studies.
A steering group with representation from PHE, BHF and NHS England met monthly to
oversee the project and were consulted at key decision points over the lifetime of the project.
Identifying CVD prevention programmes to develop as case studies
PHE included 116 current and historic programmes in their spreadsheet and SPH undertook
a hand search which identified a further two CVD prevention programmes (a total of 118
programmes). Two initial inclusion/exclusion criteria were agreed with the steering group and
Programmes which were implemented and had final follow-up completed prior to
2007 were excluded
Programmes where there was no publications published in the English language
were excluded.
From this exercise 8 programmes were selected and agreed by the CVD International
Review Steering Group which oversaw the project and comprised representatives from PHE,
BHF and NHS England. The strength and volume of evidence (factors 1 and 2) a mix of,
prevention focus (factors 3 and 4) and type of intervention (factor 5) were the most important
of the 7 factors in the selection process. Two additional case studies of national programmes
(Million Hearts and Hypertension Canada) were purposefully selected to be reviewed along
with those that met the original criteria. This is due to the particular interest of PHE and BHF
in the approach of community mobilisation and self management models used in supporting
reduction of hypertension, early detection of atrial fibrillation and high cholesterol.
Framework for organising case study information
Detailed information was gathered for each case study to populate a framework to ensure a
systematic approach. The framework used was the dynamic health systems framework (Van
Olmen et al 2012)5 which combines a range of previously published health systems
frameworks including the WHO system building blocks. This framework incorporates the
wider system elements of population, context, values and principles in addition to core health
system components of leadership and governance, health workforce, health information
systems, access to medicine and equipment, finance and service delivery.
5
Source: Van Olmen et al (2012)
Where possible, information was extracted from unpublished and published documents
readily available on the internet or through the British Library services. In addition SPH
undertook interviews with key staff for the programmes where available. This helped to fill
any significant gaps and obtain additional contextual information. The table in Appendix 1
shows the different elements of the framework and the type of content required for each
case study.
Once the information had been gathered it was organised in a consistent case study format
with two pages summarising the key points about the implementation, benefits and
limitations of each initiative. This was followed by more in depth information extracted from
peer reviewed publications.
7000.00
DALYs per 100,000 population (age standardised)
Australia
England
6000.00
France
Greece
5000.00
Ireland
Japan
4000.00
Finland
1000.00 Netherlands
Canada
0.00
Source: Global Burden of Disease Study 2016 (GBD 2016) Results. Seattle, United States: Institute for Health
Metrics and Evaluation (IHME), 2016. (http://www.healthdata.org/gbd)
Newton et al (2015) analysed the 2013 data from the GBD study, comparing potential years
of life lost from all causes across the 15 EU countries, the four UK countries, the nine
English regions, plus Australia, Canada, Norway and the USA. SPH has extracted similar
data from the GBD study for cardiovascular disease for the same countries and regions plus
Japan. The data is based on the latest information supplied by each country up to 2016.
Figure 3 shows the latest data available (2016) of age standardised years of life lost (YLL)
per 100,000 population from CVD. Years of life lost (YLL) or years of potential life lost
(YPLL) or potential years of life lost (PYLL), is an estimate of the average years a person
would have lived if he or she had not died prematurely. It is, therefore, a measure of
premature mortality. Currently CVD in Japan accounts for the fewest years of life lost per
100,000 population (1347, 95% Uncertainty Interval [UI]; 1292 - 1400) and Greece the most
(2987, 95% UI; 2770 - 3204). Of the 10 areas with the highest rate of YLL due to CVD, six
In the UK, the South East region has the lowest YLL per 100,000 population from CVD at
1724 (95% UI; 1659 - 1793) whilst Scotland has the highest YLL per 100,000 population
from CVD at 2522 (95% UI; 2320 - 2860).
Figure 4 shows the years of life lost to disability (YLD) from CVD by each country and
English region. This measure is determined by the number of years disabled, weighted by
level of disability caused by a disability or disease.
Australia
Spain
Japan
Italy
Switzerland
Canada
Portugal
Netherlands
Ireland
United States
Greater London
Denmark
West Midlands
Greece
Yorkshire and the Humber
North East England
France
England
United Kingdom
South West England
South East England
East Midlands
Northern Ireland
Wales
North West England
Scotland
Norway
East of England
Germany
Finland
Austria
Belgium
Sweden
0 100 200 300 400 500 600 700 800
Source: Global Burden of Disease Study 2016 (GBD 2016) Results. Seattle, United States: Institute for Health
Metrics and Evaluation (IHME), 2016.
Within the UK, the YLD from CVD in 2016 were lowest in Greater London at 464 per
100,000 population (95% UI; 338 - 610) and highest in the East of England at 494 per
100,000 population (95% UI; 361 - 649). Of the countries included in Figure 4, years of life
lost to disability from CVD were lowest in 2016 in Australia at 359 (95% Ul; 261 - 499) per
100,000 population compared to Sweden at 534 (95% UI; 390 - 699) per 100,000 (Figure 4).
It should be noted that the Global Burden of Disease study data is constantly being updated
and countries will frequently move up and down the rankings from year to year. It is
important to link back these snapshots in time to the overall trends shown in Figure 2. This
shows that in order to achieve rates nearer to those of Japan, France and Australia
1
Source: Public Health England (2016)
The overall national approach to CVD prevention is to focus on the risk factors in Figure 5
with initiatives that make it easier for healthy people to remain healthy and for those at high
risk or already diagnosed with CVD to change their behaviour and receive optimal medical
management to meet risk factor targets. The particular combination of population-wide
strategies and strategies targeted at high risk individuals depends on achievable
effectiveness, as well as cost-effectiveness and availability of resources. This results in a
4.Wider community
organisations working together
1.Individual
age, gender,
knowledge, skills,health
status attitudes,
behaviours
Source: Adapted from the Centers for Disease Control and Prevention (CDC), The Social Ecological Model: A
Framework for Prevention, http://www.cdc.gov/violenceprevention/overview/social-ecologicalmodel.html
There are five nested levels of the SEM which illustrate the interplay between individual,
interpersonal, local organisations, community and national influences. An approach that
The Social Ecological Model is a helpful way to understand the approach of each of the
international programmes that were chosen to develop into a case study.
Five of the case studies focus on people with high risk conditions. Those with current CVD or
a high risk of CVD are offered interventions to reduce their risk with the aim of averting
further morbidity and impact on health services. The remaining five case studies are
programmes with a combination of prevention approaches encompassing both prevention of
CVD and reducing CVD risk factors. These programmes typically comprise multiple small
initiatives under one programme umbrella.
The programme looks for ways to reduce future cardiovascular disease (CVD) risk in those
people already diagnosed with CVD or at high risk of an event. The focus is on lifestyle
change and identifying ‘treatment gaps’ where medication has not been optimised. Health
professionals, trained in the COACH system, mentor the patient on changes in lifestyle and
support them in working with their usual doctor to ensure treatment is optimised for their
particular circumstances, based on national guidance in order to reach target levels for their
modifiable risk factors.
COACH is a structured telephone and mail-out health programme for people with chronic
disease.
There are five stages to each phone coaching session:
Finding out what the patient knows: ask patients questions to find out what they
know about their risk factors and treatment for their risk factors
Education: tell patients what they should know
Patient empowerment: empower patients to ask their own doctor(s) to measure
their risk factors; provide them with their test results; prescribe appropriate
medication and alter doses/ drugs if appropriate
Action plan: set an action plan to be achieved by the next coaching session
Monitoring: check what action has taken place since the previous coaching session
and use the information as the basis for the next session.
The COACH Program runs for approximately six months with telephone-based coaching
sessions every four to six weeks. At the end of each session a letter detailing the topics
discussed is sent to the patient and the doctor(s). Patients receive a written information pack
Longer-term follow-up of RCT18 participants has shown that improvements in risk factor
status and adherence to medications following COACH are sustained for 18 months. For
example:
The percentage of patients achieving the total cholesterol target was 27% before
COACH, 57% immediately after COACH and 52% 18 months later
The percentage of patients undertaking physical activity was 70% before COACH,
94% immediately after COACH and 92% 18 months later.
A four-year follow up of RCT participants has shown that four coaching sessions over six
months is associated with significant reduction in:
Any-cause hospital admissions (by 16%)
Any-cause hospital bed days (by 20%)
Cardiac bed days (by 15%).
When assessing the published literature for the case studies COACH had more evidence
based publications outlining the benefits to patients and the health economy than any of the
other programmes. Detail of the evidence from some of these publications is outlined in the
COACH case study (Appendix 3).
Of people who attended the health check-ups and individual/group sessions, men reported:
An increase in physical activity and improved dietary pattern (9.6%)
An increase in physical activity (4.1%)
An increase in improved dietary pattern (39.3%)
No lifestyle changes (47.0%).
Women reported:
An increase in physical activity and improved dietary pattern (14.2%)
An increase in physical activity (3.8%)
An increase in improved dietary pattern (39.2%)
No lifestyle changes (42.7%).
The high risk population strategy in the FIN D2D study may be useful and applicable to
primary health care settings’ strategies relating to T2D and CVD. However, commitment to
lifestyle changes in primary health care was rather low, which is why increased motivation
and self-management of people at risk should be emphasised.
Detail of the evidence from some of these publications is outlined in the DEHKO case study
(Appendix 4).
GPs in the intervention group received one day of medical education on therapeutic targets
and strategies featured in the French guidelines on treatment of hypertension and type 2
diabetes, and were given a validated electronic blood pressure measurement device to
improve the accuracy of blood pressure measurements and a leaflet that summarised
targets and therapeutic strategies. GP participants were all members of the French National
College of Teachers in General Practice.
After two years, the proportion of patients achieving all their therapeutic targets
increased significantly in both groups, but significantly more in the intervention group
with between group OR (odds-ratio) of 1.89, (95% CI); 1.09 - 3.27, p = 0.02)
Significantly more patients achieved their blood pressure targets in the intervention
group than in the usual care group: OR 2.03 (95% CI; 1.44 - 2.88, p < 0.0001)
Systolic and diastolic blood pressures decreased significantly more in the
intervention group than in the usual care group, by 4.8 mmHg and 1.9 mmHg,
respectively (p < 0.0001 for both SBP and DBP).
The authors suggest that the absolute difference in the reduction of SBP of about 5mmHg in
the intervention group was clinically relevant because this difference could be expected to
reduce stroke mortality by 20%, and mortality related to cardiac ischaemic events or long-
term overall cardiovascular mortality by 15%.
For more detail about the evidence published from this trial see the France ESCAPE case
study in Appendix 5.
When adjusted for differences in the baseline score, the relative change in
Framingham risk score of the intervention group compared to the usual care group
was not statistically significant at -8% (95% CI; -18% to - 2%)
The difference between groups in patients reaching the low density lipoprotein goal
was 18.4% (95% CI; 5.9% - 30.9%, p=0.004)
The difference between groups in change in patients who quit smoking at 12 months
was 7.7% (95% CI; 0.4 - 14.9, p=0.038).
The cost effectiveness analysis measured societal costs, quality-adjusted life-years (QALYs)
and incremental cost effectiveness21. It concluded that the intervention in addition to usual
care does not result in QALY gain at one year, but has a small effect on vascular risk factors
and is associated with lower costs.
Treating patients at the point where they are likely to be concerned about mortality and may
be self-motivated to take action was considered to be effective and lower cost. It was seen
as productive for patient and nurse to work together collaboratively to reduce risk factors and
for patients to take responsibility for their health and be part of the solution. It is also an
opportunity to involve carers in cardiovascular risk management, rather than just surgery or
medication straight after the event.
The ability of patients to see their results online as soon as they were available was a
controversial step. One view was that patients may access results without health
professional support which could be distressing. In some areas there is a delay of a day or a
week between request to access results by the patient and the result being available to view
by them to give health professionals time to check their significance.
After the programme was finished (1 year) the functionality of the website for patients to
retrieve their own records was incorporated in to the local health electronic record system.
During the trial people could enter their own numbers, lab results from the GP, or blood
pressure taken at home, but they cannot do that in the current system.
For more detail about the evidence published about this programme see the case study in
Appendix 6.
Key outcomes:
For more detail about the CHAP programme see the case study in Appendix 7.
The basic health check-up includes: a blood pressure test, waist circumference, height and
weight, blood tests (lipids, triglycerides, HDL and LDL cholesterol, blood sugar (HbA1c,
fasting blood sugar), hepatic function, red blood cell count, haemoglobin level, and
haematocrit), electrocardiogram and urine tests for chronic kidney disease. A questionnaire
about lifestyle is focused on diet, tobacco smoking, physical activity, work life balance and
family history of disease. Results of tests are graded A to D and sent to individuals and their
employer (if the test was provided by the employer). For those at risk of CVD or metabolic
syndrome the following intervention is offered which comprises:
The use of annual health check-ups for the whole population means that individuals,
employers and health professionals can track the progress in reducing CVD risk factors and
where improvements can be made.
For more detail about the evidence published about this programme see the case study in
Appendix 8.
The programme responded to changing demographics and financial support by taking the
service to the people. For example, senior citizens initially had access to free grant-
supported buses to attend community blood pressure clinics. When this transport became
less available, the programme took the service to seniors’ group meetings. When attendance
at these meetings diminished, the programme used a donor-sponsored mobile van that took
services to a wide variety of locations including shopping centres. This mobile service
offered risk factor assessment, referral and coaching.
Part way through the 10 year programme funding period, plans for ongoing sustainability
were put in place to ensure continuation of the multifaceted approach.
Outcomes of a study assessing population-level CVD risk factors over a six year time frame
before and during project implementation are outlined in Table 1.
The October 2015 update to the 2011 Pan Canadian Hypertension Strategy detailed the
progress made so far in achieving the various 2020 targets (Table 2). Effective management
of those already diagnosed with hypertension has been more successful than the uptake of
lifestyle interventions.
Table 2: Progress towards 2020 targets set out in the 2011 Pan-Canadian
hypertension strategy
2007-2009 2010-2011 2012-2013 2020 Target
Hypertension Prevalence 19.6% 21.8% 22.6% 13%
Awareness of condition 83.4% 82.9% 84.3% 95%
Diagnosed with hypertension with 8.5% 11.1% 6.6% 40%
normal BP while not on
antihypertensive drug treatment a
(i.e. lifestyle control of
hypertension)
Appropriate drug therapy 79.9% 79.2% 79.6% 87%
Blood pressure under control 65.9% 64.1% 68.1% 78%
The core team, funded through CDC, works to distribute funding and support networks of
partners, and information gathering. Partners join the network because they have a common
aim to reduce the risk of CVD.
Organisations can apply for funding from Million Hearts for short term projects to implement
an initiative that the organisation will sustain after this time. This funding tends to be for
innovative projects such as helping health centres use their clinical data to identify potentially
hypertensive patients, or work to improve numbers of people monitoring their own blood
pressure. Funding can also be secured by taking part in the Medicare electronic health
record incentive programme that encourages meaningful use of health records to identify
people at risk of CVD and taking part in the ABCS challenge which rewards health care
providers who achieve the overall 70% target.
Features of practices and health systems that achieved high levels of ABCS and
hypertension control include:
Using multiple strategies to achieve high BP control rates aligned with the World
Health Organization’s Innovative Care for Chronic Conditions recommendations, and
strategies recommended by the Centers for Disease Control and Prevention funded
State Public Health Actions grantees and Million Hearts
Having electronic health records with features such as electronic prescribing, patient
registries, and clinical decision support tools
Implementing hypertension treatment protocols. This helps standardize and
coordinate care and facilities a team approach to BP management
Some practices were offered financial and other incentives to clinicians and patients
to encourage greater attention to BP control by health insurers
Engaging patients in BP home monitoring to assess progress, inform decision
making, and encourage adherence to treatment regimens.
For more detail about the evidence published about this programme see the case study in
Appendix 12.
Of the five programmes that focused on people with high risk conditions, COACH is
employing the greatest number of strategies (9/11) that might increase the likelihood of a
successful programme whilst ESCAPE were employing the fewest (2/11). DEHKO (7/11)
and the vascular risk programme (6/11) and Hypertension Canada (5/11) employed some
but not all of the strategies considered important for success.
Of the five community programmes, CHAP employs all 11 strategies whilst HONU and
Franklin both employ 10/11 of the strategies which might confer success. Million Hearts
utilise 7/11 and the particular case study initiative from Healthy Japan 21 employed 4/11 of
the strategies.
CVD prevention programme strategies for patient groups at high risk of a first or COACH ESCAPE DEHKO Vascular Hypertension
subsequent CVD event or diagnosis risk Canada
2 Integrate three health models: medical, public health, and health promotion
14 Develop and participate with coalitions: local, regional, state, and/or national
17 Know your community, and modify general principles to deal with local realities,
including cultural and resource issues. One size does not fit all
18 Seek reliable, long-term funding, immune from legislative and economic vagaries
19 Try to make financial and behavioural vectors point in the same direction
Ades et al (2002) considered that the thoughtful systematic application of interventions and
sustaining programme momentum, particularly in the face of economic decline, remained a
major challenge. Whilst all the case studies used some strategies included in the checklist in
Table 4, not all of the programmes have become sustainable and made the transfer to other
communities. However, three programmes, CHAP, COACH and HONU, employed the most
strategies and also focussed on sustainability. COACH and CHAP also focused on
applicability to other populations.
All the programmes employ some elements that Ades et al (2002) propose contribute to a
successful CVD prevention programme. For CVD prevention to be successful it helps if 1)
people are aware of the need and possibilities in relation to CVD reduction, 2) those at
particular risk are detected and their risk factors are identified, and 3) strategies for reducing
those risks are effective. Useful learning points from the case studies are discussed below in
relation to these three headings.
The HONU project looked at a small community and applied a multifaceted approach to
impact lifestyle and the development of healthy behaviours. HONU employed all 11
community strategies (numbers 11 to 21) from Table 4. An overarching steering group
comprising representatives from local government, large employers, chamber of commerce,
local health services, public health, schools, supermarkets and restaurants developed a
strategy to improve the health of their community. From this steering group 11 action teams
are formed who plan and implement initiatives specific to the need of their community across
all sectors. Each person on the steering group has their role written into their job description
by their employer so when anyone moves to a different job there will be a replacement on
the steering group. The steering group is also responsible for raising funding for initiatives
either by applying for national or regional funding for specific projects or raising it within the
community. Volunteers from the community were key to implementing the initiatives. The
initiatives involved activities in all sectors of the community for example; families invited to
the school domestic science rooms for cookery classes and taste testing; a range of school
based challenges for children; the offer of workplace lifestyle change courses lasting 6 to 8
This model could be an option in UK rural areas or towns where the town or district council
was keen to make a difference and where all key stakeholders could be represented. The
leadership group for each community could report into the town or district council and from
there to the local Health and Wellbeing Boards via public health teams. Well organised
communications and strong leadership from all sectors of the community were seen as key
elements to the success of the programme.
HONU was successful because there was very strong community engagement and
mobilisation and the community felt empowered to make changes that worked for them. This
empowerment in part was put in train by the initial research funding and a clear focus on
sustainability and incorporating the work into the mainstream business of the community.
Local authorities in England have a key role to develop strategy and facilitate health
improvement in the community and individually may be more or less successful in employing
some or all of the community strategies in Table 4 (numbers 11 to 21).
A focus on school and workplace support for people to undertake activities to help reduce
CVD risk factors would be helpful. There is some guidance for the NHS as an employer
(NICE, 2015) about creating healthy NHS workplaces but there could be more focus on
implementing the guidance for the benefit of employees. Some workplaces have developed
their own initiatives, giving out step counters to encourage more physical activity and offering
bike to work schemes. Overall, there is a lot of potential to develop workplace schemes
further to encourage health education sessions, physical activity, healthy eating options and
healthier ways to undertake desk based work such as standing desks and treadmill
workstations. For schools there are some marketing and teaching resources available for
teachers and some support from Sport England and the Youth Sport Trust to help people
achieve in sport however there may be other ways physical activity can be built into the
school day and a stronger focus on healthy eating and preparing healthy food across the
year groups.
It will be interesting to see the outcomes of the ‘Building Healthy Partnerships’, initiative in
eight sites in England, where funding is provided to enable Sustainability and Transformation
Partnerships (STPs) to engage with people in the community and the Voluntary, Community
and Social Enterprise (VCSE) sector to determine wellbeing and self-care priorities locally.
The self-care programme has a dual focus combining relationship building with agreeing and
implementing joint action and runs from April 2017 to June 2018.28
Many of the case studies, CHAP in Canada, HONU and Franklin County in the US, DEHKO,
in Finland, Healthy Japan 21, Hypertension Canada and Million Hearts aimed to identify
people in communities with a high risk of CVD and those with risk factors that could be
improved by lifestyle change. The promotion and implementation of an annual health check
by employers in Japan with financial incentives for high uptake, leads to a programme that
tracks most of the population every year. This top down approach can lead to employers
using the information to make work related decisions about employees depending on their
health check result and engagement with interventions offered.
Some elements of the Japan model may be less generalisable to a UK context, such as the
sharing of test results and subsequent actions with employers. A model more obviously
applicable to the UK is the one developed in Canada (CHAP). It is a community-driven and
community-owned initiative designed to be a scalable service that minimises centralised
support over time to achieve a long-term sustainable service. The basic premise is that if
people can be encouraged to come to community settings where volunteers can help them
take their blood pressure and ask them about their lifestyles to assess CVD risk in a
systematic way, then it is an opportunity to raise awareness about what their results mean
and how they can reduce their CVD risk. In this way all adults in the community can get to
know their numbers whilst detection of those at high risk of CVD and referral will improve.
This initiative ran clinics out of pharmacies who had signed up to participating in the
programme. Volunteers were recruited and trained by a nurse coordinator and clinic
sessions were held in pharmacies in rotation. In addition to education about CVD risk
factors, people have a CVD risk assessment using a questionnaire and they are assisted by
volunteers to take their own blood pressure using an automated monitor. Those meeting the
criteria for high risk of CVD and requiring treatment are referred to their GP. Those who
need to change lifestyle in order to reduce CVD risk factors are given information about what
community resources are available. The target population for the programme were those
aged ≥65 and volunteers were aged matched to this group. All those aged ≥65 were invited
to go to a session personally by the GP practice, a strategy known to elicit a higher
participation rate which is also used in the UK to invite people to take up the offer of NHS
screening (e.g. cervical, breast and bowel screening). However any adult could attend the
sessions which were advertised in the community. The CHAP model has been applied to
different communities with different requirements with the core principles being:
This case study illustrates how it can be beneficial to use wider professional groups and lay
people to deliver interventions whilst also linking the programme into primary care. This
model could be used within England, commissioned by the existing Local Authority and
Clinical Commissioning organisations or Accountable Care Systems (ACS) that are coming
on line. The service would be run by a small team such as a nurse co-ordinator and
administrative support who would run the programme by:
Recruiting pharmacies
Recruiting and training volunteers
Engaging the support of GP practices
Helping run clinics
Ensuring referrals of people with high risk of CVD were made to the relevant GP.
This is certainly feasible in England and the generic model has been employed successfully
in communities in Canada, the Philippines, in Asian communities and rural communities.
Prevention for people at high risk of a first or subsequent CVD event or diagnosis.
For people who have been identified with a high risk of a first or subsequent CVD event the
most common intervention described by the case studies was the delivery of and training of
clinical staff in one to one or group counselling and motivational interviewing. DEHKO and
Healthy Japan 21 both focussed on delivering lifestyle counselling and motivational sessions
to educate and encourage people to make lifestyle changes either as individuals or in group
settings. The Vascular Risk Management programme supported patients who had had a
CVD event with a one hour session with the vascular nurse to identify where their CVD risk
could be reduced. Patients were encouraged to make changes to their lifestyle, self monitor
and record results and changes in CVD risk factors over a period of time. A website was
developed as a resource for patients and they were able to contact the nurse and ask for
advice by email. ESCAPE focused on one day of GP training and how that translated in a
change of patient management in terms of systematically talking to patients about exercise,
diet and adherence to drug treatment and tracking changes in patient CVD risk factors. Two
national case studies Million Hearts and Hypertension Canada both emphasised training of
health professionals and adherence to guidelines. Million Hearts aimed to improve clinical
quality by choosing a limited number of evidence based interventions known to make a
difference (ABCS). They then worked with partner organisations to ensure the agreement of
standards, and the addition of data items to national data sets for surveillance and research
purposes. To ensure progression towards the standards financial incentives to meet targets,
short term funding of projects and fostering collaboration between partners has been
important.
The COACH approach has been used extensively in Australia and has the most evidence of
all the case studies with two decades of reporting on clinical and cost effectiveness. It has
been used for a range of chronic conditions but also for people at risk of developing chronic
conditions who already require medication such as people with hypertension. Once a
condition has been diagnosed, the aim of COACH is to ensure that a nurse works with the
A combination of the COACH programme where trained nurses support patients with phone
coaching and training for GPs similar to the ESCAPE case study might be a helpful
combination of initiatives to implement together. The continuing professional development
(CPD) would help refresh GPs understanding of the current UK guidance and available
prevention tools and COACH would introduce patients to self care, lifestyle change
resources, monitoring and understanding their medication. In this way the communication
between patient and GP may be more useful and support the initiative around Making Every
Contact Count in England. This would enhance the effectiveness of primary care in
facilitating patients to adhere to their medication and put in place strategies to make lifestyle
changes to reduce future CVD risk.
This approach could be commissioned by CCGs or the Accountable Care Systems that are
currently emerging in England, with CPD being offered in ways that are as accessible as
possible.
7 Conclusion
The case studies described in this report offer alternative models to CVD prevention than
those currently implemented in England. All the case studies showed some success in
reducing CVD risk factors but some programmes were more applicable and likely to be
sustainable in a UK setting than others. The most successful three programmes identified
here from the evidence available (HONU, CHAP and COACH) all have a very strong
community focus although they are targeting different elements of prevention. They are
using schools, workplaces, community centres, pharmacies, or peoples own homes to
deliver the programme. HONU has the broadest approach drawing on all sectors of the
community, whilst CHAP has a more focused approach running community clinics to detect
CVD risk factors in the local population and COACH offers support in management of risk
factors by phone to people in their own homes. Going to where the people are, empowering
individuals and the wider community with information and an understanding of CVD risk, that
they can monitor themselves, is clearly important in the success of the programmes.
All three programmes built in mechanisms for ensuring that they were sustainable in the long
term with minimal continued investment which is a particularly important consideration, given
the constraints of resources at the current time. Those case studies that were able to
achieve this, while at the same time succeeding in reducing CVD risk, are arguably the most
likely to be usefully adapted for use in England and the wider UK. They were also the case
studies that focused on long term sustainability from the outset, and we suggest that this
should be central to implementation of any changes that follow from this work in the UK.
One point that comes out strongly from many of the case studies is the large amount of
overlap between prevention of CVD and other long term non-communicable diseases, and
the fact that improvements in CVD prevention have the potential to impact on other diseases
that are currently major causes of morbidity and mortality in the UK, such as diabetes,
dementia and cancer.
7 Finances How was the intervention funded (e.g. private investment, local health commissioners, National
commissioners, Charitable)
8 Human resources Who delivers the function? (e.g. primary care physicians, nurses, consultants, local public health teams,
pharmacies, national programme staff
9 Infrastructure and supplies Are there significant back office functions? (e.g. to organise lists of people to contact, mail out
invitations to people to participate, is there any specific equipment needed? (e.g. Blood pressure monitors,
ECG machines)
Where and how is the intervention delivered (setting)? ( e.g. Clinic room in GP surgery or hospital
outpatients or ward, Community pharmacy, Village hall, phone, community centres, shopping centres,
events e.g. football matches)
10 Knowledge and Did the workforce and or volunteers need training and what for
information
How are outcomes collated and performance monitored ( e.g. locally, standard national template
collated at programme level, not at all)
Is there any monitoring about what happens to patients next?
Understanding your own risk Heart Age Test – How Healthy is Your https://www.nhs.uk/conditions/nhs-health-check/check-your-heart-age-tool/
Heart? NHS Choices
Local organisations
Local health services capacity Cardiovascular disease: risk https://www.nice.org.uk/guidance/cg181
and capability to optimise CVD assessment and reduction including
detection and management lipid modification. Updated Sept 2016,
NICE Guidance
Community
Local authority health Local health and care planning: Menu https://www.gov.uk/government/publications/local-health-and-care-planning-
promotion plans of preventative interventions. menu-of-preventative-interventions
Updated Feb 2018, PHE, Guidance
National
Food industry approach to Sugar Reduction: Achieving the 20%. A https://www.gov.uk/government/publications/sugar-reduction-achieving-the-
health to reformulation of technical report outlining progress to 20
foodstuffs date, industry guidelines, 2015 sugar
baseline levels in 9 food categories
and next steps. Mar 2017, PHE
Political will to legislate about Improving lives: the future of work https://www.gov.uk/government/uploads/system/uploads/attachment_data/fil
food, built environment, health and disability. Nov 2017, DWP e/663400/print-ready-improving-lives-the-future-of-work-health-and-
alcohol, and tobacco smoking & DoH disability.pdf
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by Department of Environment National strategy, targets and actions consultation/user_uploads/clean-air-strategy-2018-consultation.pdf
Food and rural affairs to reduce air pollution and people
exposed to emissions between 2020
and 2030.
Construction industry approach Healthy New Towns network. https://www.england.nhs.uk/ourwork/innovation/healthy-new-towns/
to healthy environments Network to develop best practice,
case studies & guidance to help
ensure all new housing developments
embed certain principles, promoting
health and wellbeing and securing
high quality health and care services
PROGRAMME AT A GLANCE
The COACH Program® (Coaching patients On Achieving
Cardiovascular Health) was developed in 1995 in Melbourne
and is currently available in all Australian states. This
prevention programme aims to reduce the impact of chronic
disease on the individual and health system.
The programme looks for ways to reduce future
cardiovascular disease (CVD) risk in those people already
diagnosed with CVD or at high risk of an event. The focus is
on lifestyle change and identifying ‘treatment gaps’ where KEY TAKEAWAYS
medication has not been optimised. Health professionals,
trained in the COACH system, mentor the patient on Started as a research
changes in lifestyle and support them in working with their project before
usual doctor to ensure treatment is optimised for their expansion to public and
particular circumstances, based on national guidance in private healthcare
order to reach target levels for their modifiable risk factors. systems throughout
Australia and other
COACH is a structured telephone and mail-out health parts of the world
programme for people with chronic disease.
Empowers and
There are five stages to each phone coaching session: supports individuals to
Finding out what the patient knows: ask patients better manage their
questions to find out what they know about their risk chronic disease and the
factors and treatment for their risk factors associated lifestyle and
Education: tell patients what they should know biomedical risk factors
Patient empowerment: empower patients to ask
their own doctor(s) to measure their risk factors; Delivered by health
provide them with their test results; prescribe professionals trained in
appropriate medication and alter doses/ drugs if the COACH system
appropriate
Action plan: set an action plan to be achieved by the Programme
next coaching session standardised across
Monitoring: check what action has taken place since training, access to
the previous coaching session and use the Program software and
information as the basis for the next session generation of
performance data
The COACH Program runs for approximately six months
with telephone-based coaching sessions every four to six
weeks. At the end of each session a letter detailing the
topics discussed is sent to the patient and the doctor(s).
Patients receive a written information pack at the start of the
programme.
The Queensland COACH Program describes the core components and distinguishing
features of the COACH Program as:
Coaches always initiate contact with the patients for coaching sessions – the programme
does not depend on the patient contacting the coach
Coaches identify where there are modifiable CVD risk factors which would improve with
lifestyle changes
Coaches identify the ‘treatment gaps’ in each patient’s management – the gaps between
the national guideline-recommended care and the care patient’s actually receive
Coaches educate, advise and encourage patients to close the ‘treatment gaps’ and
achieve guideline-recommended risk factor targets whilst working with their usual
doctor(s)
Coaches encourage patients to work with their usual doctors to achieve the most
practical medication regimens possible, in order to facilitate lifelong adherence to
recommended medication
Targets are set for reducing modifiable lifestyle CVD risk factors and closing any ‘treatment
gaps’.
Population
The programme targets people with chronic disease. If a patient has more than one chronic
disease, they are coached on the risk factors for all their conditions. There is no age limit in
the current COACH Program.
Patients in the public health system are generally recruited in hospitals, but other referral
routes are possible. For example, in the Queensland COACH Program referrals are
accepted from all sources including public hospitals, general practitioners, medical
specialists, other health professionals, cardiac rehabilitation services, ‘Quitline’ (smoking
cessation) and self-referral. In the private health system, coaches use claims information to
identify prospective patients and ‘cold call’ patients who have recently been hospitalised for
chronic diseases. 99% of patients in public health systems and approximately 80% of
people in private health systems choose to participate in the COACH Program.
Conditions included in the COACH Program include heart failure, coronary heart disease,
hypertension, stroke, type 2 diabetes, pre-diabetes and COPD. The range of conditions
covered can vary between Australian states.
COACH is a structured telephone and mail-out health programme for people with chronic
disease. A health professional trained in the COACH Program coaches patients to achieve
and maintain the target levels for their modifiable risk factors and to take the recommended
medications, according to evidence-based guidelines. There are five stages to each phone
coaching session and the cyclical process illustrated in the figure below is repeated until the
target level is achieved.
Patients receive an information pack with their first letter about their chronic condition
A nurse contacts the patient at an agreed time and delivers information and education to
help patients better manage their chronic disease. This includes discussion of biomedical
and lifestyle risk factors and setting targets based on guidelines for specific diseases
The programme runs for approximately 6 months with a call every 4-6 weeks
At the end of each telephone session, a letter detailing the topics discussed is sent to the
patient, the GP and/or their treating specialist
Patients may contact their coach for advice and support between sessions
Figure 1: The five stages to each phone coaching session. The cyclical process is repeated
until the target level is achieved
Source: Vale M. Leading the world in coaching for prevention of chronic disease. Available from
https://www.health.qld.gov.au/__data/assets/pdf_file/0028/155197/coach-factsheet.pdf (Accessed February 2018)
Outcomes
The COACH Program was originally a research project and was initially evaluated in one
single centre and one multicentre RCT with associated studies following patients for two and
four years. Further published studies have looked at outcomes for COACH compared to
usual care for private patients, outcomes for public health system patients compared to
private patients and outcomes from the COACH Program in Queensland.
COACH patients had significantly lower total cholesterol levels at 6 months follow-up
compared to usual care patients (5.00mmol/L vs 5.54mmol/L, p=0.0001)
31% of the COACH group achieved the total cholesterol target compared to 10% of the
usual care group (p<0.01)
COACH patients had significantly lower mean LDL cholesterol than usual care at 6-
months follow-up (3.11mmol/L vs. 3.57mmol/L, p=0.0004)
There was no difference in HDL cholesterol (1.12 vs. 1.16, p=0.4)
The number of patients taking lipid-lowering drugs was similar in the 2 groups (63% vs
60%). There was also no significant difference in the dose prescribed
A similar proportion of patients attended cardiac rehabilitation as part of usual care (53%
vs 50%)
At 6-months follow-up COACH patients compared to usual care only patients had:
Improvements in risk factor status and adherence to medications achieved after the COACH
Program were sustained for more than 18 months after completion of the programme.
Case-control study on COACH outcomes from the perspective of a private health insurer
(Byrnes et al (in press)
This analysis included patients aged <85 with evidence from insurance claims of a CVD
diagnosis. Outcomes based on six years of insurance hospital claims were compared for
matched patients receiving COACH plus usual care and patients receiving usual care only.
Patients in the control group were not aware that there was an intervention group. 512
patients were included in each group and were matched for age, sex, relationship status and
prior hospital admission history (minimum 12 months history). The average age of
participants was 75 years and approximately 70% of each group were male.
There were significantly fewer deaths in the COACH group (21.9%) than the usual care
group (16.8%) (absolute reduction in all-cause mortality of 5.08% (95%CI -9.91 to -0.25,
p=0.04)
There was a significant reduction in mortality for males receiving COACH compared to
usual care (hazard ratio 0.70 (95%CI 0.53 to 0.93, p=0.014). The difference for females
was not significant
A comparison of results for public health system and private patients (Jelinek et al 2014)
Australian patients in private hospitals are usually of higher socio-economic status than
those treated in public hospital systems. This study compared outcomes for 2,266 patients
treated in in public hospitals in two states with outcomes for 3,278 patients from four private
health funds throughout Australia. The socioeconomic status of the two groups was
confirmed by postcode analysis.
Greater improvements in the risk factors occurred in the public health group than in the
private health group. These improvements were statistically significant for fasting blood
glucose, body weight, smoking, physical activity, total and LDL cholesterol and diastolic
blood pressure.
Table 4: Proportion of people taking medications before and after the COACH
programme for CHD and type 2 diabetes.
CHD patients Diabetes patients
Before After Before After
COACH COACH COACH COACH
Statin 92% 93% 66% 78%
Beta-blocker 72% 72% 27% 28%
Antiplatelet agent 92% 93% 52% 59%
ACE inhibitor/ angiotensin receptor 77% 78% 63% 68%
antagonist
The COACH Program provides training and evaluation data for coaches, who are employed
by healthcare organisations.
Finances
The programme is delivered in-house by participating healthcare organisations.
A private insurer analysed the cost impact for matched patients who underwent COACH plus
usual care (n=512) compared to usual care alone (n=512).
The average COACH Program cost per participant was $592 (£333)
The average net cost impact to the insurance company of the COACH Program
compared to usual care over a 6.35 year follow-up period was a saving of $12,115 per
person (£6,822)
There was a significant difference in health care costs between COACH patients who
received ≥4 coaching sessions ($42,307; £23,826) and usual care patients ($61,725;
£34,754); a difference of $19,418 (£10,931) per person (p=0.006). This difference was
not significant for patients with ≤3 coaching sessions
There was a significant difference in health care costs between male COACH patients
($47,680; £26,842) and male usual care patients ($66, 627; £37,509); a difference of
$18,947 (£10,667) per person (p=0.029). This difference was not significant for female
patients
(March 2016 costs, Australian dollars. Sterling costs calculated using March 2018 exchange
rate)
The use of the COACH Program in the public health system is funded by the state
government health departments.
The randomised controlled trials assessing the impact of COACH were funded by project/
research grants.
Human Resources
The programme is delivered by qualified health professionals trained in the COACH system.
Full time coaches can take on 200-250 new patients per year.
In the initial single centre study assessing the impact of the COACH Program, the first
coaching session was the longest in duration with a median time of 20 minutes (range 5 to
45). Subsequent coaching calls were a median of 10-11 minutes long (range 3 to 66).
In the multicentre study assessing the impact of the COACH Program the median duration of
the first coaching session was 30 minutes (range 6 to 200). The duration of subsequent calls
was 20 minutes (range 5 to 50).
Experienced coaches can undergo the ‘Train-the-Trainer Coach Course’ to become a trainer
of novice coaches and conduct quality assurance activities.
Data
The COACH Program Software Application provides all key performance indicator data on
the effectiveness of the programme. It includes patient baseline characteristics, patient
uptake, discontinuation rates, achievement of guideline-recommended biomedical and
lifestyle risk factor targets and adherence to guideline-recommended medications at entry to
and exit from the programme. Relevant medical guidelines are incorporated in to the
software application and are updated as guidelines change.
Organisations delivering the COACH Program receive six-monthly evaluation reports which
include comparison with the national mean. Results are provided for individual coaches and
organisations. The evaluation reports are used to review operations and improve the
outcomes within each organisation through a continuous quality improvement process.
The COACH Program software also produces written summaries of each coaching session
which are sent to patients and their doctor(s) and act as a record of progress. These are
structured with headings which address each risk factor with the actual result, recommended
treatment, target and whether the patient is meeting the target. Risk factor charts allow
patients to track their progress towards achieving their risk factor targets.
REFERENCES
Byrnes J. Elliott T. Vale MJ. Jelinek MV. Scuffham P. Coaching patients saves lives
and money. The American Journal of Medicine. December 2017 (epub ahead of
print)
Health Support Queensland. The COACH program® fact sheet. Available from
https://www.health.qld.gov.au/__data/assets/pdf_file/0028/155197/coach-
factsheet.pdf (Accessed February 2018)
Jelinek MV. Santamaria JD. Best JD. Thompson DR. Tonkin AM. Vale MJ. Reversing
social disadvantage in secondary prevention of coronary heart disease. International
Journal of Cardiology 2014, 171: 346-350
Jelinek M. Vale MJ. Liew D. Grigg L. Dart A. Hare DL. Best JD. The COACH
Program produces sustained improvements in cardiovascular risk factors and
adherence to recommended medications – 2 years follow-up. Heart, Lung and
Circulation 2009, 18: 388-392
Ski CF. Vale MJ. Bennett GR. Chalmers VL. McFarlane K. Jelinek MV. Scott IA.
Thompson DR. MJA 2015, 202(3): 148-153
Vale M. Leading the world in coaching for prevention of chronic disease. Available
from http://www.adma.org.au/Day1/Margarite%20Vale.pdf (Accessed February 2018)
Vale MJ. Interview with SPH, February 2018
Vale MJ. Jelinek MV. Best JD. Dart AM. Grigg LE. Hare DL. Ho BP. Newman RW.
McNeil JJ. Coaching patients on achieving cardiovascular health (COACH): a
A CASE STUDY
PROGRAMME AT A GLANCE
DEHKO, was launched in Finland as part of the Finnish
National Diabetes Programme, established as a ten year
programme running from 2000 to 2010 and aimed to improve
self-care and prevent and reduce complications from type 2
diabetes. From 2011, the DEHKO programme expanded to
include raising awareness and reducing risk of non-
communicable diseases with common risk factors including
cardiovascular disease (CVD), dementia, chronic obstructive
pulmonary disease (COPD) and type 2 diabetes. This
programme ‘One Life’ is supported by a collaboration of the
Finnish Diabetes, Brain and Heart Associations and focuses on
supporting people to make lifestyle changes to improve
modifiable risk factors.
DEHKO aimed to prevent type 2 diabetes and diabetes related complications and conditions;
to improve the quality of diabetes care and to support the self-care of people with diabetes.
DEHKO has supported the whole population strategy, but the main thrust of the project is on
a high risk population strategy.
From the outset of the programme, diabetes was treated as a serious cardiovascular risk
factor; “The second most important task is to agree upon measures to reduce the risk of
CVD among people with type 2 diabetes – requiring a substantial change of attitude by the
decision makers in the healthcare field and the care providers. The central message is that
type 2 diabetes is by no means a “mild diabetic disease” but a fatal cardiovascular disease if
all the risk factors are not properly treated.” (Development Programme for the Prevention
and Care of Diabetes in Finland, 2000-2010’, Tampere 2001).
The DEHKO programme was co-ordinated by the Finnish Diabetes Association, working with
primary health care, specialised medical care, occupational health care, and the National
Public Health Institute. It included FIN-D2D, a special programme for the prevention of type
2 diabetes.
From 2011, the DEHKO programme became ‘One Life’, which encompassed the Finnish
Diabetes Association, Finnish Brain Association and the Finnish Heart Association. The
programme was aimed at raising awareness in the whole population about all risk factors for
common non communicable diseases including CVD, dementia, COPD and diabetes, with a
focus on prevention, health promotion and seeing the person as a whole.
Population
Current figures according to the Finnish Diabetes Association website (March 2018) are that
Finland has a population of 5.5 million. They estimate that there are 50,000 people with type
1 diabetes and about 300,000 people with type 2 diabetes in Finland. About 4,000 children
under the age of 15 have diabetes. The number of undiagnosed cases of type 2 diabetes is
estimated at 150,000. Approximately 10% of the population has diabetes.
Whole population strategy aims to prevent metabolic syndrome and the risk factors for
type 2 diabetes and targets the whole population DEHKO has supported the whole
population strategy but the main thrust of the project is on a high risk population strategy.
High Risk population strategy aims to prevent and delay the development of type 2
diabetes in individuals at high risk with a focus on close relatives of individuals with type
2 diabetes, women with a history of gestational diabetes, individuals with hypertension or
elevated blood glucose or a disturbance of fat metabolism or metabolic syndrome,
individuals with overweight or central obesity
‘One Life’ incorporates both the whole population strategy and high risk population strategy
for those at high risk of CVD, type 2 diabetes, COPD and dementia.
Service Delivery
Whole population strategy
One of the programme goals was to raise awareness of diabetes and its risk factors in the
whole population through various activities such as media campaigns and health fairs. No
further information was available on how awareness raising through these routes was
achieved.
There was a population wide promotion of screening using the modified Finnish Diabetes
Risk Score test (FINDRISC) which can be completed through health care units,
pharmacies, the internet and public campaign events.
People eligible for the intervention were those who scored ≥15 points in the FINDRISC
or had a history of ischemic cardiovascular events, gestational diabetes, impaired fasting
glycaemia (IFG) or impaired glucose tolerance (IGT). They were offered support to
reduce their future T2D risk. The initial intervention was an in depth health check-up.
Health check-ups included:
o in depth questionnaires about life style (tobaccos smoking, physical activity, diet)
o an oral glucose tolerance test
o a test for levels of total and high density lipoprotein cholesterol
o a measurement of systolic and diastolic blood pressure (mm Hg)
o use of antihypertensive medication, verified from prescriptions if possible
Framingham Risk Score (FRS) was calculated for those ≥30 years and for those ≥45 the
10 year CVD mortality risk (Systematic Coronary Risk Evaluation (SCORE) was
calculated.
Participants were offered the opportunity to participate in individual or group-based
lifestyle counselling in primary health care setting conducted by local nurses. The goal
was to encourage them to change their lifestyle in the recommended direction and
recognise risk factors in their own lifestyle.
The topics of the individual counselling sessions were based on needs, and the focus
was on physical activity, meal frequency, alcohol, fat and fibre intake, salt use, weight
and smoking.
The group sessions included weight maintenance and exercise groups and lectures on
diabetes and lifestyle changes.
Staff were given training for the purpose and for the practical implementation of the
program. The programme was promoted in healthcare units which referred people into
the programme.
One Life, established in 2011 after DEHKO ended, has been established on many of the
same principles as DEHKO, with some developments. The programme has not been
formally evaluated but discussion with a Project Manager at One Life provided some
overview of aims and achievements:
People have said that they lack money and time for their health, so there is an effort to
show that this need not be an obstacle. One Life provides concrete aids to support small
decisions that people make about their health every day e.g. small cards to deliver in
seminars where people are sitting for a long time, reminding them to spread their feet,
move around in their chair
One Life organise a Health for All day, which includes a ‘dream day of exercise’, usually
10th May, which might include going to the gym, hiking, climbing etc. Around 2,000
people are thought to have organised an event that day
Workplaces are engaged, and currently 800 workplaces receive a newsletter every
Monday morning outlining exercises and ideas for health. People who attend the
workplace activity are sent further information about how to improve their health
‘Dream Day of work’ is normally held on 5th October and encourages workplaces to
promote workers’ health. Activities include webinars, sharing a healthy breakfast
together, exercise tasters, competitions, etc.
Where the general public has been targeted, the focus has been on people at risk or who
already have diabetes, heart disease or a brain related illness:
Gestational diabetes courses are run for pregnant women. This is a free 3 week web-
based course on health, diet, exercise and relaxing. The course runs monthly and there
are 50-60 attendees on the course at a time
There is a three week web-based course for women who have previously had
gestational diabetes. The course runs every second month, and is very popular, with
around 250 people on the course at a time
For people newly diagnosed with type 2 diabetes there is a nurse-run web-based course.
The course is available to 30 people at a time, and they are able to discuss lifestyle, diet
and exercise.
The web courses were viewed by One Life as one of the most effective interventions.
The courses are of good quality, engagement is high and feedback has been positive
Campaigns in the community have included targeting high blood pressure. Events
where people can have their blood pressure measured have been popular. In 2017,
100,000 people had their blood pressure measured during a one week campaign
Finnish television is required to offer public health associations some time slots for free,
which One Life has used.
The intention is to give people realistic and achievable goals. Social media has been a good
way to share conversations and experiences.
Some interventions are targeted at healthcare providers. They are often given ‘stories’,
by patients, of what it is like to live daily life with diabetes or heart disease and how those
people might wish to be treated. Small workshops are delivered and tools provided
Dialogue with decision makers is key. They are supportive, but financial considerations
are very important. They understand that prevention is cheaper and One Life provide
examples and evidence to demonstrate this at both regional and national level e.g.
around cycling in Helsinki, where 100km of cycle path has been built and One Life were
able to prove that it was cheaper to build those than to deal with illness.
More recently, in addition to heart, brain and diabetes, the work of One Life has also
incorporated respiratory health and mental health, as many of the risk factors and solutions
are shared. One Life continues the work of the DEHKO diabetes programme in the
prevention and care of diabetes. There is a stated effort to further work to make
rehabilitation and peer support an integral part of care and there are sub-projects that stress
the pursuit of:
Rehabilitation and peer support as part of the care of type 1 and type 2 diabetes,
bringing vascular risks under control and promoting lifelong vascular health
Gaining control over diabetes expertise by ensuring versatile health communications and
awareness raising and producing measures with tools, training publications and
guidelines
Outcomes
Whole Population strategy
A study carried out a survey of people to understand if DEHKO had any impact of raising
awareness and self-reported lifestyle changes in Finnish middle-aged population. (Wilkstrom
et al 2015).
‘Health Behaviour and Health among the Finnish Adult Population’ is a postal survey
conducted annually by the National Institute for Health and Welfare. To facilitate the
evaluation of the FIN-D2D, questions regarding diabetes prevention programme and self-
reported changes in health habits were included into the survey in the years 2004-2008.
Based on these questions, it was possible to assess the change in public awareness of
diabetes prevention and T2D risk factors over the lifespan of the FIN-D2D project. The
participants aged over 35 years were included in this analysis. The dataset included 5,007
men and 5,975 women. After excluding participants with missing data on awareness of
diabetes prevention programme (n=151), the final dataset included 10,831 men and women.
In the FIN-D2D area 25% (347/1384) of men and 48% (797/1674) of women reported
being aware of the programme
In the control area, the proportions were 20% (702/3,551) and 36% (1,514/4,222),
respectively
The overall awareness increased among both genders and in all areas during the project
period, but the level of awareness was consistently higher in the FIN-D2D area
Female gender and higher age were associated with increasing awareness of the
programme in both areas
Self-reported lifestyle changes were more common among women, but associated with
the level of awareness of the programme more often among men than women
Researchers concluded that the awareness of diabetes and its risk factors increased among
men and women in both implementation and control areas during the FIN-D2D project
period. The activities of the implementation project may at least partly explain the
differences in lifestyle changes between areas, especially among men. The results suggest
that health promotion campaigns increase the population awareness about the prevention of
chronic diseases and as a result, especially men may be prompted to make beneficial
lifestyle changes.
Table 1 presents the mean baseline estimated 10 year risk for CVD events and mortality
estimated by risk-calculators. During the one-year follow up the FRS decreased in women
and the SCORE decreased in men.
9.6% of the 1052 men reported both an increase in physical activity and improved dietary
pattern
4.1% of 1052 men reported an increase in physical activity
39.3% of 1049 men reported an improved dietary pattern
47.0% reported no lifestyle changes
14.2% of the 1995 women reported both an increase in physical activity and improved
dietary pattern
3.8% of the 1995 women reported an increase in physical activity
39.2% of 1995 women reported an improved dietary pattern
42.7% reported no lifestyle changes
The estimated 10-year risk for CVD events decreased 3.5% in men and 1.5% in women
reporting an increase in physical activity and improvement in diet, compared to an increase
of 0.15% in men (p<0.001, between groups) and decrease of 0.43% (p=0.027, between
groups) in women with no lifestyle changes after adjustment for age and baseline
Framingham Risk Score.
Numbers needed to treat to prevent one CVD event by lifestyle changes were 25 for men
and 59 for women.
Researchers concluded that lifestyle counselling offered in primary health care for one year
resulted in beneficial changes in dietary pattern and physical activity, which were associated
with a reduction in the estimated 10-year CVD event risk, but not with reduction in estimated
Separate analysis was carried out of the impact of the intervention on women with
gestational diabetes (GDM) (Riatio et al 2014).
‘One Life’ is a joint initiative in partnership with the Finnish Brain Association, the Finnish
Diabetes Association and the Finnish Heart Association. DEHKO has continued to focus
primarily on diabetes as the broader ‘One Life’ programme has been implemented and there
is coordination between the groups leading the programmes to ensure economies of scale
and consistent messaging.
Finances
The Finnish Government supports the DEHKO and other diabetes programmes with revenue
generated by Finland’s Slot Machine Association (RAY).
The financing for the FIN-D2D Project (2000–2007), which targeted the obese, at-risk
population and included screening and lifestyle counselling, early diagnosis, and treatment,
came from a variety of sources: RAY, the five district hospitals engaged in the project, the
Ministry of Social Affairs and Health, the National Public Health Institute, and the Finnish
Diabetes Association.
Human Resources
No information was available
The Diabetes Centre in Tampere organise a number of counselling and training courses for
people with diabetes, their family members and health care professionals and estimate that
1 600 people attend these each year.
Education and further training for health care professionals include several seminars and
basic and advanced courses. Tailor-made education and counselling are also offered for
health care professionals.
The staff responsible for courses, training and education at the Diabetes Centre includes two
physicians, four nurses, two nutritionists, one psychologist, a chiropodist, a physical activities
instructor, an exercise planner, kitchen personnel, two course secretaries, an education
manager and an education secretary.
Data collection
The Health Behaviour and Health among the Finnish Adult Population survey is an annual
postal survey conducted by the National Institute for Health and Welfare. The primary
purpose is to obtain information on the current health behaviour of the working-age
population with a self-administered questionnaire. The survey examines key aspects of
health behaviour such as food habits, physical activity, smoking and alcohol consumption
and includes questions on participants’ sociodemographic background and medical history.
To facilitate the evaluation of the FIN-D2D, questions regarding the diabetes prevention
program and self-reported health habits were included in the survey in the years 2004-2008.
PROGRAMME AT A GLANCE
ESCAPE, conducted in France from 2006 to 2008, was a
pragmatic cluster randomised controlled prevention trial. It
was designed to show whether a multifaceted intervention,
aimed at general practitioners (GPs), could significantly
increase the proportion of hypertensive patients at high risk of
cardiovascular disease (CVD) who achieved all their
recommended therapeutic targets.
The primary endpoint for this programme was the change in the proportion of patients
achieving all of their therapeutic targets at two years.
Three therapeutic targets were defined for patients without type 2 diabetes: BP ≤ 140/90
mmHg, LDL ≤ 3.36 mmol/l, and no smoking.
Five therapeutic targets were defined for patients with type 2 diabetes: BP ≤ 130/80 mmHg,
LDL ≤ 2.59 mmol/l, HbA1c ≤ 7%, no smoking, and a prescription for low-dose aspirin.
Key secondary endpoints were the change in the proportion of patients achieving each of
their individual targets and the values for BP, LDL, and HbA1c.
Other secondary endpoints were the variation in the Framingham-Anderson score for
coronary risk, the occurrence of the first clinical cardiovascular event (validated by a
committee blinded to randomization), change in antihypertensive drug prescriptions, and
quality of life.
There was an intention to address the ‘diagnosis and treatment gap’ by targeting health
providers and moving the focus from lack of patients’ adherence.
The approach was pragmatic using existing resources and guidance but requiring more
consultation and, potentially, prescription/ treatment.
Population
This was a national programme, involving 257 GPs in clusters randomised by region, from
23 colleges that were all members of the French National College of Teachers in General
Practice (CNGE).
A total of 905 patients received the intervention, and 927 received usual care: analysis at
primary endpoint was 860 for usual care group and 860 for intervention.
GPs were asked to include the first eligible patients they saw over a week, with a minimum
of seven patients.
Exclusion criteria:
Patients were not eligible if:
Recruitment of GPs:
Eleven colleges (173 GPs) were randomised to the usual care group and 12 (162 GPs)
to the intervention group
Attendance at the one-day training in the intervention group or the 90 minute-meeting in
the usual care group was mandatory for GPs to include patients
145 GPs (90%) in the intervention group attended the one-day training, of which 126
(87%) recruited at least one patient in the trial
144 GPs (83%) in the usual care group attended the 90 minute-meeting, of which 131
(90%) included at least one patient
The characteristics of the active GPs were similar in both groups in terms of gender, age,
type and duration of practice
The mean number of patients recruited per GP was 7.1 (minimum = 1, maximum = 16)
Recruitment of patients:
Between November 2006 and July 2007 1,832 patients were included in the trial, 927 in
the usual care group and 905 in the intervention group
On average they were 62 (standard deviation (SD) 7.8) years old, and the sex ratio of
men to women was 2:1. All patients were receiving treatment for prevention of CVD, had
been treated for hypertension for an average of 10.9 years (SD 8.1), and 71% had more
than two other cardiovascular risk factors associated with hypertension. The average
body mass index was 30.5 kg/m2. The average diabetes duration of the 1,047 patients
with type 2 diabetes was 7.5 years (SD 6.5)
At baseline patient characteristics were comparable in both groups, except for systolic
BP (SBP) and diastolic BP (DBP), which were significantly higher in the intervention
Service Delivery
The programme ran for a two year fixed period from 2006 to 2008.
One day of medical education for GPs, including some focus on the therapeutic targets
and strategies for achievement, featured in the French guidelines on hypertensive and
type 2 diabetes (T2D) patients' care
An electronic blood pressure (BP) measurement device for GPs
A leaflet for GPs summarising the guidelines
Four prevention dedicated consultations for each patients twice a year, performed by the
GP. During these, the GP was to negotiate drug changes if guidelines targets were not
achieved, and systematically assess patient's compliance, dietetics, exercise, and
smoking issues if needed
Feedback for GPs on patients' results at baseline and at 1 year follow-up
Outcomes
The programme was evaluated by a pragmatic cluster randomised trial comparing
intervention (n=905), GPs having attended training, offering patients 6 monthly consultations
focused on optimizing treatment and discussing lifestyle, versus usual care (n=927). A total
of 1,832 high-risk (of CVD) hypertensive patients were included.
The primary endpoint for this programme was the change in the proportion of patients
achieving all of their therapeutic targets at two years.
Three therapeutic targets were defined for patients without type 2 diabetes: BP ≤ 140/90
mmHg, LDL ≤ 3.36 mmol/l, and no smoking.
Five therapeutic targets were defined for patients with type 2 diabetes: BP ≤ 130/80 mmHg,
LDL ≤ 2.59 mmol/l, HbA1c ≤ 7%, no smoking, and a prescription for low-dose aspirin.
Key secondary endpoints were the change in the proportion of patients achieving each of
their individual targets and the values for BP, LDL, and HbA1c.
Other secondary endpoints were the variation in the Framingham-Anderson score for
coronary risk, the occurrence of the first clinical cardiovascular event (validated by a
committee blinded to randomisation), change in antihypertensive drug prescriptions, and
quality of life.
Key results:
After two years the proportion of patients achieving all their therapeutic targets increased
significantly in both groups, but significantly more in the intervention group: Between
group OR (odds-ratio) 1.89, (95% confidence interval (CI) 1.09 to 3.27, p = 0.02)
Significantly more patients achieved their blood pressure targets in the intervention
group than in the usual care group: OR 2.03 (95% CI 1.44 to 2.88, p < 0.0001)
Primary endpoint
Due to missing values at every time point, the primary endpoint could not be modelled for six
patients; therefore, the analysis for the primary endpoint was based on 1,826 patients. Over
two years of follow-up, the proportion of patients achieving all of their therapeutic targets
increased in both groups, but the increase was significantly higher in the intervention group:
OR 1.89, 95% CI 1.09 to 3.27, p = 0.024 (Table 1). Similar trends were observed in patients
with and without type 2 diabetes, but did not achieve statistical significance.
Table 1 Primary outcome: changes within groups and differences between groups at
month 24 (M24) in the proportion of patients achieving all their therapeutic targets
Endpoint Group M0 n/N (%) M24 n/N (%) OR (95% CI) P OR (95% CI) P-
for within for between value
group group
All patients 3 Intervention 56/900(6.2) 110/860(12.8) comparison
3.23(2.12 to <0.001 comparison
1.89(1.09 to 0.024
or 5 targets 4.94) 3.27)
Hypertension Intervention 7/527 (1.3) 24/526 (4.6) 3.90 (1.60 to 0.003 2.36 (0.68 to 0.175
+ T2D (5 0.52) 8.18)
targets)
Usual care 9/520 (1.7) 14/513 (2.7) 1.65 (0.69 to 0.262
3.98)
Hypertension Intervention 49/373 86/334 (25.8) 3.12 (1.94 to <0.001 1.63 (0.99 to 0.120
(3 targets) (13.1) 5.03) 3.01)
Secondary endpoints
Individual therapeutic targets
The proportion of patients achieving their BP targets did not change significantly in the usual
care group. However, significantly more patients in the intervention group achieved their BP
targets at two years. The difference between the two groups was significant: OR 2.03, 95%
CI 1.44 to 2.88, p < 0.001 (Table 2). The proportion of patients achieving their targets for
LDL and not smoking increased in both groups, with no significant difference between the
groups. There was no change in the proportion of patients with HbA1c ≤ 7% in either group
in the type 2 diabetes sub-population.
Other endpoints
SBP was reduced by 1.2 mmHg in the usual care group and by 6.0 mmHg in the
intervention group. The 4.8 mmHg difference between the two groups was statistically
significant, in favour of the intervention group (p < 0.001). Similarly, for DBP, the
difference between the groups at the end of the trial was 1.9 mmHg, statistically
significant in favour of the intervention group (p < 0.002)
At baseline the Framingham-Anderson scores were comparable in the two groups and
decreased by 1.2% in the usual care group and by 2.2% in the intervention group over
the 2 year period. The difference between the two groups was statistically significant in
favour of the intervention group (p < 0.001)
Antihypertensive drugs
At baseline the average number of antihypertensive drugs per patient was similar in the
two groups, 2.16 (SD 1.04) in the intervention group and 2.18 (SD 1.04) in the usual care
group. After two years, this number increased in both groups but increased significantly
more in the intervention group: 2.41 (SD 1.05) versus 2.29 (SD 1.06) in the usual care
group, (p = 0.020). In addition, significantly more patients in the intervention group
received at least one additional antihypertensive drug over the two-year study period
than in the usual care group (p = 0.009)
Cardiovascular events
During the study 89 cardiovascular events were reported, and 61 were validated using
patient records by a committee blind to randomization. The incidence of the first
cardiovascular event was 3.0% in the intervention and 3.7% in the usual care groups, (p
= 0.513)
Quality of life
Changes in scores for physical and mental quality of life were very small and not
significantly different between the two groups
Finances
The study was funded by unrestricted research grants from the French National College of
Teachers in General Practice, Takeda France, and Merck-Serono, France.
Human Resources
The physicians were all GPs and were members of the French National College of Teachers
in General Practice (CNGE). Firstly, all the 33 French regional colleges belonging to the
CNGE were invited to participate in ‘a randomized trial with hypertensive patients’. Twenty
three of these colleges agreed to participate. Eight hundred and seventy-seven GPs,
members of these 23 colleges, were contacted by each regional research leader by
telephone and/or Email, or during a usual meeting, and 335 agreed to participate.
Data
Outcomes were collated locally by GP:
o At baseline, and every six months for two years along with usual follow-up, the GPs
in both groups collected patients’ clinical and biological data
o Prescriptions of drugs for hypertension and metabolic treatment were reported at
baseline and 24 months
Questionnaires were given by GP to patient, and responses sent directly to ‘data
treatment centre’: At inclusion, 12-months and 24-months, patients of both groups were
given a sealed envelope containing five short questionnaires on quality of life (SF-8),
adherence, diet, exercise, and smoking habits to be completed at home and sent directly
to the data treatment centre in a pre-paid envelope
REFERENCES
Pouchain et al.: Effects of a multifaceted intervention on cardiovascular risk factors in
high-risk hypertensive patients: the ESCAPE trial, a pragmatic cluster randomised
trial in general practice. Trials 2013 14:318.
A CASE STUDY
PROGRAMME AT A GLANCE
The programme, based in the Netherlands, assessed the
effectiveness of adding internet-based, nurse-led vascular
risk factor management to usual care for patients with
clinically manifest vascular disease. Eligible patients,
recruited between 2008-2010, had a recent clinical
manifestation of a vascular disease and a number of risk
factors that were not at the recommended levels.
PROGRAMME EXPERIENCES
BENEFITS AND OUTCOMES
The ability of patients to see their results
The relative change in Framingham online as soon as they were available was
Risk score of the intervention group a controversial step. One view was that
compared to the usual care group patients may access results without health
was not statistically significant when professional support which could be
adjusted for differences in patient distressing. In some areas there is a delay
attributes of a day or a week between request to
access results by the patient and the result
Larger percentage differences being available to view by them to give
between groups were seen in health professionals time to check their
reaching the LDL recommended significance.
levels (18.4% 95%CI 5.9 to 30.9,
p=0.004) and quitting smoking After the programme was finished (1 year)
(7.7% 95%CI 0.4 to 14.9, p=0.038), the functionality of the website for patients
but there was no significant to retrieve their own records was
difference between groups for other incorporated in to the local health
risk factors electronic record system. During the trial
people could enter their own numbers, lab
The cost effectiveness analysis results from the GP, or blood pressure
measured societal costs, quality- taken at home, but they cannot do that in
adjusted life-years (QALYs) and the current system.
incremental cost effectiveness. It
Other features of the programme including
concluded that the intervention in
an extended outpatient appointment to
addition to usual care does not
review risk factors and ongoing
result in QALY gain at 1 year, but
communication to review progress in
has a small effect on vascular risk
changes to modifiable risk factors have
factors and is associated with lower
been incorporated into the usual care of
costs
patients. Nurses can set up this system of
enhanced support if they think it might be
Treating patients at the point where
effective for patients coming through the
they are likely to be concerned
CVD outpatients department after an
about mortality and may be self-
event.
motivated to take action was
considered to be effective and
lower cost
The premise of the programme is that a large proportion of patients with a clinical
manifestation of a vascular disease are still at high residual cardiovascular risk due to not
reaching treatment targets.
Treatment of vascular risk factors by nurse practitioners has been found to be effective, but
is costly and time consuming for patients and health care professionals. Delivery of the
programme via the internet was tested as a low cost method of support compared to regular
clinic attendance.
Population
Patients were recruited from two centres in the Netherlands. 638 patients were invited to
participate and 330 were randomised.
Eligible patients were aged 18 to 80 with a recent clinical manifestation of a vascular disease
e.g. myocardial infarction, stroke or peripheral arterial disease. Patients had to have at least
two of six treatable risk factors that were not at target levels. These risk factors were:
Patients also had to have access to internet at home, be able to read and write Dutch, and
be independent in daily activities. Patients with an estimated life expectancy of <2 years or a
malignant disease were excluded.
Service Delivery
Patients were recruited between October 2008 and March 2010. At the start of the
programme patients had a one hour outpatient appointment where they received information
on their risk factor levels. Participants randomised to the intervention group received
instructions about the internet programme and a username and password for their
personalised website.
Patients were asked to complete a questionnaire by internet every three months to report
newly diagnosed diseases and hospital admissions. When a cardiovascular event was
suspected, medical records were retrieved and assessed. Patients were invited to a follow-
up appointment at 12 months. The nurses conducting the follow-up measurements were
blinded to the patient’s group.
A personalised website focusing on the patient’s risk factors that required additional
treatment. This included an overview of the status of all risk factors (green=at goal;
yellow=close to goal; red=needs attention) and drug use
A separate internet page for each risk factor with a history of risk factor measurements,
drug use, treatment goal, advice from the nurse, correspondence between the nurse and
patient and news items for that particular risk factor
Patients were asked to log in at least every other week to submit new measurements
(blood pressure, weight, smoking status, cholesterol) and to read and send messages
Patients were encouraged to measure their own blood pressure at home or ask their
general practitioner to measure their blood pressure. The nurse posted patients
laboratory forms for blood tests to measure plasma lipids and glucose
Prescriptions for changes in drug regimen were posted to patients
Patients were sent a summary of a news item by email every other week, to prompt the
patients to visit their website
The internet programme was provided in addition to usual care provided by the treating
hospital physician and the general practitioner
Usual care was provided by the treating hospital physician and the general practitioner and
was based on the 2006 Dutch cardiovascular risk management guideline. The physician and
general practitioner were informed of the patient’s risk factor status.
Outcomes
Randomised controlled trial (RCT)
The programme was evaluated by a multicentre prospective RCT comparing intervention via
the internet in addition to usual care (n=155) versus usual care alone (n=159) (Vernooij et al
2012). The mean (standard deviation (SD)) age was 59.9 (8.4) and 75% were male. 16 (5%)
patients dropped out during the study and did not have follow-up measurements.
Key results:
The relative change in Framingham risk score of the intervention group compared to the
usual care group was statistically significant at -14% (95%CI -25% to -2%)
Adjusted for differences in the baseline score, the relative change in Framingham risk
score of the intervention group compared to the usual care group was not statistically
significant at -8% (95%CI -18% to 2%)
The difference between groups in patients reaching the low density lipoprotein goal was
18.4% (95%CI 5.9% to 30.9%, p=0.004)
The difference between groups in change in patients who quit smoking at 12 months
was 7.7% (95%CI 0.4 to 14.9, p=0.038)
There was no significant difference between groups for other risk factors
Hazard ratio for vascular events 0.66 (95%CI 0.35 to 1.24) (not statistically significant)
152 of 155 patients in the intervention group logged in to the website with a median of 56
(interquartile range 35 to 83) logins during the year
131 patients entered a median of 7 (3 to 14) measurements during the year, mostly
blood pressure and weight
The monthly number of logins reduced during the 12 months from a maximum of 1,099
logins in month three to 435 logins in month 12
134 patients sent a median of 14 (7 to 22) messages
Patients using the website more often tended to have the highest Framingham scores at
baseline (highest CVD risk) and had the largest improvements
During the 12 month period the nurse practitioner used a mean (SD) time of 23 (12)
minutes per month per patient
Measures
The Framingham heart risk score represents the 10 year risk for coronary heart disease. A
10% change was considered to be the minimal clinically relevant difference.
At a threshold value of €20,000 for each QALY gained, there is a 65% probability that
nurse-led, internet-based intervention is cost-effective
No significant difference was found in health benefit in terms of QALYs (mean 0.86 for
the intervention group vs 0.85 for usual care)
Table 2: Cumulative mean costs (in €) for patients during the 12 month programme
(Greving et al 2015)
Intervention Usual care Difference
Medical costs:
GP consultation 151 142 +9
Complementary medicine 13 6 +7
practitioner consultation
Paramedic healthcare 192 294 -102
professional consultation
Specialist consultation 353 333 +20
University hospital inpatient days 249 935 -685
General hospital inpatient days 421 462 -41
Medication 451 464 -13
Internet-based vascular 220 0 +220
management programme
Subtotal medical costs 2,052 2,635 -583
Indirect non-medical costs:
Absence from paid work 2,289 1,675 +614
Reduced productivity at paid work 326 566 -240
Absence from unpaid work 159 164 -4
Subtotal indirect non-medical 2,775 2,405 +370
costs
Total costs 4,859 5,078 -219
The study received ethical approval from the University Medical Center Utrecht and the
Rijnstate Hospital Arnhem.
Finances
The programme was funded by a grant from ZonMw, The Netherlands Organization for
Health Research and Development.
The cost of the 1-year internet-based vascular risk factor management programme was
€220 (2009 prices) per patient.
Human Resources
The nurse practitioner personalised the website for each patient depending on the presence
of risk factors that needed additional treatment. This took an average of 10 minutes.
The nurse practitioner could view all pages for all patients and could see an overview of the
current status and last log-in attempts and new messages sent. The treating nurse logged in
every working day and replied to messages, and sent messages to patients who were not
using the programme at least every other week. In cases of non-response the nurse
contacted patients by phone. During the 12 month period the nurse practitioner used a mean
(SD) time of 23 (12) minutes per month per patient.
At the start and end of the programme patients had a one hour outpatient appointment.
Further contact between the patient and nurse practitioner in the intervention group was
through the internet.
Costs
A cost-effectiveness analysis was completed alongside the randomised controlled trial.
REFERENCES
Greving JP. Kaasjager HAH. Vernooij JWP. Hovens MMC. Wierdsma J. Grandjean
HMH. van der Graaf Y. de Wit GA. Visseren FLJ. Cost-effectiveness of a nurse-led
internet-based vascular risk factor management programme: economic evaluation
alongside a randomised controlled clinical trial. BMJ Open 2015, 5: e007128
Vernooij JWP. Kaasjager HAH. van der Graaf Y. Wierdsma J. Grandjean HMH.
Hovens MMC. de Wit GA. Visseren FLJ. On behalf of the SMART study group.
Internet based vascular risk factor management for patients with clinically manifest
vascular disease: randomised controlled trial. BMJ 2012, 344: e3750
A CASE STUDY
PROGRAMME AT A GLANCE
The Cardiovascular Health Awareness Program (CHAP) was
developed in Ontario, Canada. CHAP aims to improve the
process of care related to the cardiovascular health of older
adults.
CHAP started as a research study piloting a community
based model of cardiovascular disease (CVD) prevention in
two communities. CHAP encourages older people to
become more aware of their cardiovascular risk and to
acquire self-management skills. Key elements are: KEY TAKEAWAYS
Free cardiovascular risk assessment and education
sessions held in community pharmacies A community-driven
Family physicians invite their patients over 65 to and owned initiative
attend and sessions are also advertised in the local
community Using aged matched
Sessions are run by volunteer peer health educators volunteers considered
Community Health Nurses train the volunteers, very important for the
provide quality control and are on call to assess community intervention
people with elevated blood pressure to be seen as peer
During the sessions volunteers assist patients to take advice not medical
and record their blood pressure using an automated advice
device and complete a CVD risk profile (based on
blood pressure, previous hypertension diagnosis and Use of personalised
lifestyle risk factors) invitation letters
Patients are told about the importance of reducing resulted in the highest
lifestyle CVD risk factors and signposted to attendance numbers
community agencies and resources for support
Family physicians receive feedback on patients Designed as a
attending sessions scalable, sustainable
service that can be
CHAP is a community-driven and community-owned tailored to different
initiative. It is designed to be a scalable service that target groups
minimises centralised support over time to achieve a long-
term sustainable service. Since it began, the CHAP model
has also been applied in a range of different types of
communities where it is tailored to maximise participation
from the target group. For example:
South Asian community in Ontario, Canada
Rural community in Alberta, Canada
Social housing developments in Ontario, Canada
Rural community in the Philippines
The objective of CHAP is to improve the process of care related to the cardiovascular health
of older adults in Ontario, Canada and shift the distribution of risk at the population level.
The CHAP programme integrates primary care and existing community resources to provide
cardiovascular risk assessment including repeated accurate measurement of blood pressure
among older adults. CHAP aims to overcome poor/selective uptake and improve follow-up
(‘closing the loop’).
CHAP was developed as a low cost, community-driven initiative with the aim of minimising
centralised support over time to achieve a long-term sustainable community-owned
programme. CHAP is designed to be:
Population
Thirty nine communities in Ontario involved, not including two communities where the
programme was piloted. The total population in 2005 was 973,246 including 140,642 people
aged ≥65 years. Community size ranged from 10,000 to 60,000. Communities had five or
more family physicians and two or more pharmacies. Currently nine of the communities have
integrated CHAP as one of the regular community programmes.
In the study assessing the effectiveness of CHAP, 20 communities were allocated to receive
CHAP and 19 communities acted as controls. People aged ≥65 years were invited to attend
community pharmacy CHAP sessions. Family physicians were asked to identify people who
had visited their practice at least once in the last 12 months and who were community
dwelling and mobile.
Service Delivery
The CHAP working group was originally formed in 2000. The components of the CHAP
programme were developed through various pilots and community-wide demonstrations to
develop a standardised programme implementation guide with a toolkit of downloadable
resources and templates.
Outcomes
Multiple publications present details of the programme and its implementation and outcomes
from early implementation in 2003 to roll-out to 20 CHAP areas. The CHAP programme was
also evaluated through a cluster randomised controlled trial (in 2006) and there has been
ongoing work looking at wider implementation.
Early outcomes of the community health awareness program in 2003 (Chambers et al 2005)
56 sessions held in 27 community pharmacies
79% of eligible pharmacies and 47% of eligible family physicians participated in CHAP
983 of 2,493 invited patients (39%) attended a session. 59% returned for a 2nd pharmacy
session. Average age 74.8 years, 53% female. All patients agreed for their results to be
sent to their physician
Positive feedback from volunteers and pharmacists
Pharmacies
Challenge: Busy environment with high levels of customer traffic. Solution: Attempted to
set up sessions in unobtrusive areas
Challenge: Limited or inadequate space. Solution: recruited alternative pharmacies or
worked within constraints
Patients
Challenge: Tendency to arrive all at the same time, at the start of sessions. Solution:
Divided sessions into two time slots
Challenge: Lack of adherence to protocol (i.e. patients talked or moved whilst blood
pressure being taken). Solution: Reinforced need for volunteers to monitor patients
Findings of the community cluster randomised trial of CHAP with impact on hospitalisations
(Kaczorowski et al 2011)
Twenty communities randomised to provide CHAP and 19 communities to no intervention
controls. Communities stratified by population size and geographical location. In CHAP
communities residents aged ≥65 were invited to volunteer to run cardiovascular risk
assessment and education sessions (also known as awareness sessions) held in community
pharmacies over a 10 week period (see below for further details). In both arms, usual health
promotion and care services were available to residents. The primary outcome was a
composite of hospital admissions for acute myocardial infarction, stroke and congestive
heart failure in the year before and year after CHAP. Relative rates were calculated (event
rates for intervention communities compared to control communities):
The mean age of residents in both intervention and control communities was 75 and the
mean proportion of men was 43% in both groups
Exposure to CHAP was associated with a 9% relative reduction in the composite primary
endpoint (rate ratio 0.91, 95%CI 0.86 to 0.97, p=0.002) or 3.02 fewer annual hospital
admissions per 1,000 people aged ≥65
There were also statistically significant reductions favouring the intervention for acute
myocardial infarction (rate ratio 0.87, 95%CI 0.79 to 0.97, p=0.008) and congestive heart
failure (rate ratio 0.90, 95%CI 0.81 to 0.99, p=0.029)
There was no significant difference for stroke (rate ratio 0.99, 95%CI 0.88 to 1.12,
p=0.89)
When calculated as number of unique people admitted to hospital there was a significant
difference favouring CHAP in those with newly prescribed antihypertensive drug
treatment (rate ratio 1.10, 95%CI 1.02 to 1.20, p=0.02)
There was no significant difference in all-cause mortality (rate ratio 0.98, 95%CI 0.92 to
1.03, p=0.38) or in-hospital death from CVD (rate ratio 0.86, 95%CI 0.73 to 1.01, p=0.06)
In the year after the intervention public health units and agencies in the study areas were
contacted to assess potential co-intervention or contamination from any other
cardiovascular health initiatives during the study period. No other such initiatives were
identified
Longitudinal cohort study on the impact of CHAP in reducing blood pressure for people
attending CHAP sessions between 2008 and 2010 (Ye et al 2013)
This study included 13,596 people who attended CHAP sessions between 2008 and 2010.
Sessions were delivered weekly in 22 communities after the completion of the cluster RCT
using the same CHAP process. Participants were divided into three groups for analysis:
attendance at one session (n=9,531), attendance at two sessions (n=1,567), attendance at >
The proportion of patients with high blood pressure at baseline was 28.8% who attended
1 visit, 27.4% for those attending 2 visits and 32.2% for those attending >2 visits
For participants with initially high blood pressure, systolic blood pressure (SBP) dropped
by 0.79% and diastolic blood pressure (DBP) by 0.71% every month in CHAP (SBP ratio
0.992, 95%CI 0.991 to 0.994, p<0.01; DSP ratio 0.993, 95%CI 0.991 to 0.994, p<0.01)
Average blood pressure for the high blood pressure group improved from 142/78mmHg
to 123/69mmHg over the 18-month period
The authors reported that a decrease in blood pressure of 10/5mmHg reduces the risk of
developing heart failure by about 50%, stroke by 38%, heart attack by 15% and death by
10% (referencing Hypertension Canada)
There was no significant change in SBP and DBP for people without high blood pressure
at baseline
Older adults who lived alone, had hypertension at baseline, reported healthier eating
habits and presented with a higher SBP at baseline were more likely to attend more than
one session
The CHAP Working Group provided centralised support at all stages of programme delivery,
including a launch meeting, weekly teleconferences with local coordinators, monthly
newsletters, an interactive web forum and site visits to assist with recruitment and promotion.
Programme coordination was done by Local Lead Community Organisations.
The use of a cluster RCT to evaluate the programme required consistency of delivery across
the 20 sites. However, standardisation needed to be balanced with flexibility to varying
contexts and resources of individual communities e.g. in support, processes, materials and
resources.
Finances
A 2005 publication states that the programme is funded in part by the Canadian Institutes of
Health Research, by a contract with the Ministry of Health and Long-Term Care,
Government of Ontario and by The Team for Individualizing Pharmacotherapy in Primary
Care for Seniors. The Kidney Foundation is also acknowledged for contributions in kind for
coordinating older adult volunteers.
CHAP programme development: Ontario Stroke Strategy and Ontario Ministry of Health
Promotion - $2.3 million 2004-2011
CHAP evaluation: Canadian Stroke Strategy ; Canadian Institutes of Health Research;
Host organisations including Institute for Clinical Evaluative Science - >$2 million 2001-
2012
In the cluster RCT, lead organisations were asked to submit proposals for up to $5,000 in
funding to lead a 2-month community mobilisation phase (26 agencies from the 20
Funding agreements were re-negotiated during the project in several cases to respond to
local challenges and circumstances (figures not provided).
Average cost $30,494 per community (£17,007) across all intervention communities
Cost varied from $11,976 to $57,113 (£6,680 - £31,855) depending on community size,
internal volunteer support and availability of ‘in-kind’ infrastructure support
CHAP central costs $804,304 (£448,521) – an average of $40,215 (£22,425) per
community for a one year time period
Overall this equated to approx. $71,000 (£39,591) per community or $20.20 (£11.26) per
older adult resident
The additional cost of the CHAP intervention (i.e. $20.20perresident)was offset by slightly
lower health care costs in the intervention communities such that the total cost in the year
after the intervention was equal in both groups at approximately$4200perelderlyresident
(mean cost difference -$1.69; 95%CI -$156.76 to -$152.39; p= 0.982).
Costs from a CHAP Pragmatic Trial (screening, referral, education, pharmacy support for
elderly hypertensives) to reduce CVD hospital admissions plus death from any cause: $1.4
million in 2007 (£780,678); cost per patient $10 (£5.58) for 140,642 over 65 year olds or
$110 (£61.33) for 13,379 screened.
Human Resources
Community pharmacies provided awareness sessions using volunteer peer health educators
and mentors with support from community health nurses and community-based family
physicians. Volunteers included retired nurses, (about 50% of the volunteers), health
professionals trained outside of Canada, and aspiring medical students.
Pharmacists were asked to hold at least two CHAP sessions. Volunteers were asked to
attend at least two awareness sessions (in addition to training sessions).
Two regional coordinators, each covering 10 CHAP communities, provided regular support
to local CHAP coordinators who were responsible for operating CHAP in their respective
communities. CHAP sessions at different pharmacies were scheduled on different days.
The contribution of family physician opinion leaders was seen as fundamental in achieving a
high rate of participation by family physicians. Actions included sending personalised letters,
speaking at hospital rounds and/or contacting colleagues directly to discuss potential
concerns/questions.
Community pharmacy awareness sessions run by volunteers required the recruitment and
training of volunteers in the use of blood pressure monitors.. Volunteers were recruited by a
peer health educator coordinator through liaison with community organisations, seniors
groups and advertising in local media.
GPs were also required to send invitation letters sent to people aged ≥65, identified and
were reimbursed for this activity.
An ‘enhanced educator’ training module was created to support skill development for
volunteers with a background or interest in providing additional health resources and peer-
counselling. This training was not consistently delivered due to time constraints.
Data
Data collected at pharmacy awareness sessions are sent to a computerized database (run
by a data management company), with patient consent. The software prepares a tailored
patient report that is sent to the family physician. These reports rank patients by their most
recent systolic blood pressure within diagnostic/treatment groups (i.e. potentially new cases
of hypertension, and potentially under-treated, non-adherent patients) and reflect different
blood pressure targets for patients with diabetes. Family physicians also get an overview
report six months later with the percentage of patients in their practice with high blood
pressure and who reached systolic blood pressure target levels compared to other
anonymised practices.
The pharmacist on duty during CHAP sessions documents consultations with high-risk
patients using a standardised form focusing on determining whether high blood pressure
was due to sub-optimal drug therapy or adherence issues.
In addition:
REFERENCES
Carter M. Karwalajtys T. Chambers L. Kaczorowski J. Dolovich L. Gierman T. Cross
D. Laryea S. for the CHAP Working Group. Implementing a standardized community-
based cardiovascular risk assessment programme in 20 Ontario communities. Health
Promotion International 2009, 24(4): 325-333
Chambers LW. Dolovich L. Kaczorowski J. Thabane L. on behalf of the CHAP
working Group. Session on Primary Care and Chronic Diseases: ICES
Cardiovascular Research Day. June 2012
Chambers LW. Kaczorowski J. Dolovich L. Karwalajtys T. Hall HL. McDonough B.
Hogg W. Farrell B. Hendricks A. Levitt C. A community-based program for
Cardiovascular Health Awareness. Revue Canadienne de Santé Publique 2005,
96(4): 294-298
Kaczorowski J. Interview with SPH, February 2018
Kaczorowski J. Chambers LW. Dolovich L. Paterson JM. Karwalajtys T. Gierman T.
Farrell B. McDonough B. Thabane L. Tu K. Zagorski B. Goreree R. Levitt CA. Hogg
W. Laryea S. Carter MA. Cross D. Sabaldt RJ. Improving cardiovascular health at
population level: 39 community cluster randomised trial of Cardiovascular Health
Awareness Program (CHAP). BMJ 2011, 342:d442
Ye C. Foster G. Kaczorowski J. Chambers LW. Angeles R. Marzanek-Lefebvre F.
Laryea S. Thabane L. Dolovich L. The impact of a cardiovascular health awareness
program (CHAP) on reducing blood pressure: a prospective cohort study. BMC
Public Health 2013, 13: 1230
Goeree R, vonKeyserlingk C, , Burke N, , He JKaczorowski, J Economic Appraisal of
a Community-Wide Cardiovascular Health Awareness Program VA L U E IN HE
ALTH 1 6 ( 2 0 1 3 ) 3 9 – 4 5
Population
This is a national programme targeted at the whole population from age 1 year, all whom are
eligible for annual health check-ups.
Service Delivery
Healthy Japan 21 included 70 specific goals in nine focus areas; six related to lifestyle and
three directly related to high risk conditions for CVD. These were: diet and nutrition, physical
activity and exercise, leisure and mental health, smoking, alcohol, dental health, diabetes,
cardiovascular disease and cancer.
This particular case study focuses on offering lifestyle change interventions for people who
have been identified via the annual health check to have a high risk of CVD or metabolic
syndrome.
Where people did not meet the following target values, lifestyle change interventions were
offered:
3.High FBG
BMI <25kg/m2
No Written information
No Written information
1 risk Yes or no
BP, Blood pressure, FBG, Fasting blood glucose, BMI, body mass index
Written information
Regardless of the presence/absence of the need of lifestyle intervention, written information
is supplied to all people receiving this specific health check-up once a year (simultaneously
with notification of the check-up results). It provides information tailored to individual subjects
based on the health check-up data and responses to the questionnaire filled in at the time of
the check-up.
The person is guided to take actions towards achieving their goals during a session lasting
20 minutes or more. If it is a group session this takes 80 minutes or more (eight individuals
or less per group) at which an action plan is prepared.
On the basis of the specific health check-up data and the results of the questionnaire carried
out to determine the status of lifestyle (smoking, exercise, diet, rest, etc.), support is
provided by a one to one or group session and the results (evaluation made six months
after the date of preparation of the action plan) are evaluated.
On the basis of the specific health check-up data and results of the survey carried out to
determine lifestyle status (smoking, exercise, diet, rest, etc.), support sessions are provided,
and the progress of the action plan implementation (interim evaluation) and the results (six
months after the date of preparation of the action plan) are evaluated.
The facilitator explained the necessity of lifestyle improvement, the relationship between
lifestyle and the specific health check-up data, the patient's lifestyle, knowledge about
metabolic syndrome and lifestyle-related chronic diseases, and the influence of these
factors on the daily lives of the individuals receiving the motivational support
Explanation was given about the advantages of lifestyle improvement and the
disadvantages of failing to improve lifestyle
The facilitator suggested changes needed to improve the lifestyle (e.g. diet and exercise)
The facilitator set goals for actions and the timing of the outcome evaluation,
accompanied by a discussion of the social resources available and needed for lifestyle
improvement
The facilitator showed how to measure body weight and abdominal circumference
Goals for actions and the action plan were prepared by the individual receiving the
motivational support under guidance via the sessions
A follow-up session was undertaken if helpful for the participant and thought beneficial by
the facilitator
The evaluation was made via interview or other method (telephone, e-mail, etc.), six
months after the first session
Outcomes
One nationwide cohort study (Nakao et al 2018), looked at the effectiveness of these lifestyle
change interventions offered to people identified as being at high risk of metabolic syndrome
and cardiovascular disease. Known as the Metabolic Syndrome and Comprehensive
Lifestyle Intervention Study (MetS ACTION-J), researchers used the data from the National
Database of Health Insurance Claims and Specific Health Check-ups of Japan (NDB). The
national data captured examination records and laboratory data to diagnose metabolic
syndrome (MetS). Anonymised data regarding subjects who underwent a health check-up
between year 2008-09 and 2011-12 from the Ministry of Health, Labour and Welfare
(MHLW) was extracted. The main findings are:
Clinically relevant reductions, i.e. >5% at year 3, were achieved in a significantly higher
percentage of participants of the lifestyle intervention compared to non-participants
(Waist circumference (WC), 21.4% vs 16.1% and BMI, 17.6% vs 13.6%; p<0.001, each)
Higher weight reductions (>10%) were also observed in a significantly higher percentage
of participants
Both abdominal and overall obesity, measured by categorical weight reductions,
improved significantly more in participants compared to non-participants
Participants who received lifestyle intervention had significantly more improvements in
MetS, as compared with non-participants who did not receive a lifestyle intervention
Further results from the National Health and Nutrition Survey are available from the website
of Health Japan 21. The second phase started in 2013 with new targets for 2022 which are
outlined in the table below.
Table 2 National Health and Nutrition Survey results and targets to 2022 (Udagawa K
2008)
Measure 2010 2011 2012 2013 2014 2015 2022
target
Average SBP pressure 138 138 137 138 137 136 134
(mmHg) men 40-89 years
Average SBP (mmHg) 133 133 131 133 132 130 129
women 40-89 years
Total cholesterol >240mg 13.8% 10.7% 10.8% 11.3% 12.0% 10.4% 10%
/dL men 40-79 years
Total cholesterol >240mg 22.0% 20.3% 17.5% 19.9% 20.2% 20.9% 17%
/dL women 40-79 years
LDL cholesterol >160mg 8.3% 8.0% 7.5% 8.4% 7.6% 8.3% 6.2%
/dL men 40-79 years
LDL cholesterol >160mg 11.7% 13.6% 11.0% 11.7% 12.8% 12.7% 8.8%
/dL women 40-79 years
Mean salt intake (g) 10.6 10.4 10.4 10.2 10.0 10.0 8.0
(adults >20 years)
Mean daily intake 282 277 287 283 292 294 350
vegetables (g) (adults
>20 years)
Smoking (adults >20 19.5% 20.1% 20.7% 19.3% 19.6% 18.2% 12%
years)
Individuals who regularly 26.3% 25.9% 26.5% 22.3% 20.9% 24.6% 36%
exercise men 20-64 years
Individuals who regularly 22.9% 24.8% 21.5% 19.4% 17.5% 19.8% 33%
exercise women 20-64
years
Individuals who regularly 47.6% 47.4% 49.6% 47.6% 42.4% 52.5% 58%
exercise men >65 years
Individuals who regularly 37.6% 36.2% 39.4% 37.8% 35.7% 38.0% 48%
exercise women >65
years
Number of restaurants that supply 17284 n/a 21163 23322 25388 30000
food products low in salt and fat
SBP, systolic blood pressure, LDL, low density lipoprotein, BMI, body mass index
Specific plans for the promotion of health were to be formulated in the manner best suited to
the local area by enlisting the co-operation of residents and various community health
organisations to promote the plan.
Finances
Local governments assumed the main responsibility for financing health promotion. A
financial adjustment policy was implemented in the form of financial assistance from national
to local governments, to account for variation in the availability of local revenues. This policy
aimed to balance revenues of local governments and ensure a minimum level of public
health services was provided equally across the country.
In April 2008, a decision was made to finance disease prevention with Japan’s social health
insurance scheme that aims to help individuals to have control over their own health. The
universality of social health insurance coverage is an important factor for Japan.
Social health insurance also facilitates effective integration of health promotion into health
service delivery and financing arrangements.
Human Resources
Health promoting leaders have been identified and nominated by community members and
trained to conduct health promoting activities in their communities. These include advocacy
of healthy lifestyle, behaviour, attitudes, dietary habits, access to health-related information
and improvement of health literacy and education at community level. Studies suggest that a
community participation approach suited to the socioeconomic setting has been effective in
improving health-related behaviour and promoting health in Japan.
This is conducted every November by the Ministry of Health, Labour and Welfare. 300
survey districts are randomly selected through Japan, each district with approximately 30
households. All household members aged >1 year are invited to participate. Public health
centres of local governments are responsible for conducting the survey.
Population
At the start of the programme in 1970, Franklin County Maine was a rural, low income
population of 22,444. In 1990-92 the population was 29,008 and in 2010 the population was
30,768. The population was predominately white. The residents become older and poorer
over the 40 years follow-up, but the ratio of population to primary care physicians improved.
All adults were eligible to participate in the programme.
The 15 other counties in Maine were used as comparators. The population of Maine was
992,048 in 1970, 1,227,928 in 1990-2 and 1,328,361 in 2010.
Service Delivery
The programme started in 1970 and emphasised education and detection using a
community-based clinic model with nurses and trained community volunteers sent into town
halls, churches, schools, grocery stores, restaurants, pharmacies, dental and medical offices
and workplaces:
Nurses reviewed personal and family history, symptoms, medications and lifestyle and
measured weight, blood pressure and non-fasting serum cholesterol
Each encounter ended with personal counselling
People with uncontrolled health conditions were referred to physicians for treatment
Ongoing results of patient monitoring were sent to the patient’s physician and entered
into the programme database
Programme elements
Hypertension: In the 1970’s the programme emphasised the detection and control of
hypertension with at least monthly clinics in each county town. More than 200 health
coaches and volunteer nurses provided multifactorial, integrated cardiovascular risk
factor education, screening, referral and follow-up of all adults in age groups in diverse
settings. There was active follow-up with patients and primary care physicians by mail,
telephone and home visits to improve tracking and control
Healthy eating: From the outset, the programme promoted healthy eating. Volunteer
citizen and professional task forces initiated, promoted and staffed diverse projects
including community-wide heart healthy menu campaigns involving restaurants, schools
and grocery stores, nutritionist-guided healthy grocery tours and consultations with
school food services to serve heart-healthy meals
Physical activity: From the outset, the programme promoted physical activity. The local
university added a community health education department and, aided by a community
fund drive, built a health and fitness centre in 1992 with the area’s only indoor pool, open
to students and community residents. Programme staff helped open school facilities for
indoor adult walking, make outdoor recreation areas smoke-free, produced and
distributed brochures on local, year-round fitness opportunities and mapped safe walking
routes
Hyperlipidaemia: In 1986 a programme was added to detect and control
hyperlipidaemia. This used the same community outreach model as the hypertension
programme, using three person teams of patient, clinician and nurse. In 1986,
programme nurses also began risk factor coaching in selected physician practices
Smoking: In 1988, a programme was added to minimise tobacco use with a number of
initiatives between 1988 and 2011. Teachers and 50 volunteer health professionals
collaborated in developing and delivering in-class tobacco-related curriculum. State-wide
and national tobacco guidelines and initiatives were adopted locally e.g. adult, youth and
clinician education, community organisation and advocacy, public policy change (i.e.
smoke-free areas) and individual and group intervention. Programme staff, together with
motivated high school students, conducted tobacco sales ‘sting’ interventions on under-
age tobacco sales, with education and follow-up of all regional tobacco product sources
Complex patients: In 2000, a programme was added to co-manage diabetes in medical
practices. This was a collaborative nurse care management programme facilitating care
for complex patients with lipid disorders, diabetes and/or heart failure. The programme
was later integrated with all hospital-affiliated primary care physician practices
The programme responded to changing demographics and financial support by taking the
service to people. For example, senior citizens initially had access to free grant-supported
buses to attend community blood pressure clinics. When this transport became less
available, the programme took the service to seniors’ group meetings. When attendance at
these meetings diminished the programme used a donor-sponsored mobile van that took
services to a wide variety of locations including shopping centres. This van provided risk
factor screening, referral and coaching.
Outcomes
Mortality
Franklin County age and income adjusted mortality rates decreased below Maine
mortality rates during 1970 to 2010, with the greatest differences coinciding with peak
programme activities
From 1970-89 Franklin County mortality rates were the lowest in Maine (observed vs
expected difference -60.4 deaths/100,000; 95%CI -97.9 to -22.8, p<0.01))
From 1990-2010 Franklin County’s household income decreased relative to other Maine
counties but they still had significantly lower mortality than predicted by income
(observed vs expected difference -41.6 deaths/ 100,000; 95%CI -77.3 to -5.8, p=0.005)
Figure 1: Age adjusted total and heart disease death rates for Franklin county and
Maine (1960 to 1994) with Franklin program phases (Record et al 2000)
Hypertension
The proportion of people with treated and controlled hypertension increased from 18.3% in
1974/5, to 43.0% in 1977/8; an absolute increase of 24.7%; 95%CI 21.6% to 27.7%, p<0.01.
Hyperlipidaemia
The proportion of people with treated and controlled cholesterol levels improved from 0.4%
in 1986 to 28.9% in 2009; an absolute increase of 28.5%; 95%CI 25.3% to 31.6%, p<0.01.
From 1986 to 2010 people with more visits were more likely to have treatment for high
cholesterol that resulted in reaching the recommended levels.
Smoking
Smoking quit rates (ever smokers who reported they had quit) improved from 48.5% in
1994/5 to 69.5% in 2006-10
Quit rates were significantly higher for Franklin County compared to the rest of Maine
from 1996-2000 (observed vs expected difference 11.3%; 95%CI 5.5% to 17.7%,
p<0.01)
Quit rates were significantly higher for Franklin County compared to the US
Participation rates
Encounters with programme staff averaged 5,000 per year from 1974 to 1994 and 3,000
per year afterwards
There were over 150,000 encounters by 2010; an average of more than 5 encounters
per resident
In 1974, the RHA, with hospital medical staff sponsorship, established the community-wide
Franklin Cardiovascular Health Program. Leadership was provided by a nurse manager,
medical director and diverse advisory groups.
Over time, many local public and non-profit organisations collaborated on various
components of community efforts. Participants included the hospital, local businesses,
schools, and the University of Maine, which developed a health education degree
programme and trained local Community Action Agency outreach workers.
Continuous quality improvement became the standard operating procedure for regional risk
factor identification and management at individual, population and programme levels. The
programme promoted adherence to national guidelines and guideline based information
systems.
Finances
Funding came from grants (averaging $20,000 annually), client donations and modest fees
for services. Annual budgets averaged $50,000 during 1986-1994, excluding volunteer
efforts and in-kind contributions.
Federal support from 1972 to the mid-1980s came from the Office of Economic Opportunity
and the Rural Health Care Service Outreach grant programme. The programme received
multiple small grants of $10,000 to $80,000, mostly during the initial 20 years, from the
Federal Health Underserved Rural Area grant program, the Bingham Program, the Regional
Medical Program, Maine Bureau of Health, Maine Department of Human Services grants,
Western Maine Community Partnership, the Healthy Communities Coalition, Franklin
Memorial Hospital and the United Way. Federal grants also funded planning and
implementation of a comprehensive capitated health insurance plan for 3,000 indigent
residents.
During the years when regional businesses (often paper and wood mills) thrived, employers
paid for screening, follow-up and coaching services for their employees and helped institute
effective non-smoking policies. When the mills were sold to more distant owners there was
less cooperation with the programme.
Costs
The lower than expected hospitalisation rates were associated with $5,450,362 (£3,919,300)
reductions in total in-and out of area hospital charges for Franklin County residents per year.
Human Resources
Data
Medical record systems provided aggregated data from 1974 to 2009 on screening and
follow-up encounters, demographics, behavioural risk factors and hypertension and
cholesterol control. Additional data was available from routinely collected sources such as
census and local and national disease control centres.
REFERENCES
Record NB. Onion DK. Prior RE. Dixon DC. Record SS. Fowler FL. Cayer GR. Amos
CI. Pearson TA. Community-wide cardiovascular disease prevention programs and
health outcomes in a rural community, 1970-2010. JAMA 2015, 313(2): 147-155
Record NB. Harris DE. Record SS. Gilbert-Arcari J. DeSisto M. Bunnell S. Mortality
impact of an integrated community cardiovascular health program. Am. J Prev Med
2000, 19(1): 30-38
PROGRAMME AT A GLANCE
New Ulm is a small community of 17,000 people. Local
health organisations were keen to track the cardiovascular
health of the population before and during the
implementation of community wide interventions. The Health
of New Ulm (HONU) project implemented individual, family
and community level interventions in order to influence KEY TAKE AWAYS
behaviour and reduce modifiable cardiovascular disease
(CVD) risk factors. HONU gathered cardiovascular risk data Long term whole
either from electronic records or from community based CVD population approach to
risk assessments held 3 times a year in New Ulm. prevention
People at risk of CVD or with pre-diabetes were
assigned a health coach to support lifestyle change The project worked with
Families were invited to come together once a month individuals, families,
and do physical activity and cook together and take workplaces, food
part in taste testing outlets and local
government for
HONU worked with employers to support them to
multifaceted approach
offer health and wellness activities in the workplace
to prevention
A systematic method was used to assess how
nutritionally healthy all food outlets were and
Mid way through the10
supported a shift to more healthy options including
year funding period
smaller portion sizes
(2009 to 2019) a
HONU implemented community health challenges sustainable system was
around diet and activity set up so the
The project worked with local government on community could
integrating a health approach when planning continue the work once
changes to the built environment funding had ended
Safe walking and cycling routes to school and other
school based activities were promoted to parents and Consistent well
children organised
communications and a
Part way through the programme funding period, plans for
strong leadership team
ongoing sustainability were put in place to ensure from all sectors of the
continuation of the multifaceted approach. community were key
elements to success of
the programme
Population
The health promotion campaign was targeted at the rural Minnesota communities of New
Ulm (population 13,500), Springfield (population 2,215) and Sleepy Eye (population 3,600).
The priority population is described as adults aged 40 to 79 living in New Ulm, which has a
total population of 16,759 and 7,855 residents aged 40 to 79 years. This population is 98%
white and insurance levels are high (an estimated 8.7% residents <65 years lack insurance).
The 2009 CVD risk assessment programme was free to adults who resided or worked in the
target community of New Ulm, which had a working age population of about 10,000.
Service Delivery
Between 2009 and 2013 a range of interventions were delivered.
Community Interventions
Heart Health Screenings: Free to all adults and conducted in 2009 (5,221 screened)
and 2011 (3,215 screened). Participant recruitment for the 2009 screening programme
was through media adverts, direct mail and email, physician referral, website, social
media and announcements by employers and community groups. Screening events
were held at community and workplace locations. Screening involved a 30 minute visit
where participants completed a health survey and had anthropometric (e.g. BMI) and
blood biomarkers collected. Participants received a CVD risk report, including
information on lifestyle risk factors and guidance for medical follow-up as required.
Participants also received health coaching on creating goals for lifestyle risk factors and
were referred to available community or programme-specific resources to help achieve
those goals
Community Health Summits: Annual community-wide events focused on lifestyle
changes with national motivational speakers. Attendance ranged from 250 to 700 per
year
Three formal run/ walk events per year: 5 and 10 km distances with participation
ranging from 150 to 600 per event
Six Community Health Challenges: Using broad annual campaign themes varying in
duration from 6-8 weeks to 12 months. These encouraged small manageable changes
related to physical activity, healthy eating, weight management and stress management.
Enrolment ranged from 539 to 2,236
Workplace Interventions
Workplace Assessments: Assessment of wellness policies and environment
completed by 46 businesses. Recommendations made e.g. workplace smoking and
nutrition policies.
o 89% employers now promote community programmes and resources for health –
prefer community programmes to workplace programmes
o 72 workplaces engaged in LOSE IT to WIN IT with 1,500 participants
o 116 employers now engaged in some level of wellness programme (previously in
2009 only 5 of largest 100 employers had a wellness programme)
o 5,703 participants in workplace programmes through to December 2013
Free Heart Health Screenings conducted at workplaces: Aggregate reports given to
participating workplaces showing prevalence of risk factors among employees and
providing recommendations for wellness programmes targeting those risk factors
Workplace Behavioural Change Programmes: Short (6-8 week) and long (12 month)
behaviour change programmes focused on weight loss, nutrition, self-care and exercise.
14 programmes implemented at 95 workplaces from 2009 to 2013 with 4,879 employees
participating. 24 educational presentations with 1,287 employees at 16 companies and
freedom from smoking classes conducted at 2 workplaces
Outcomes
Outcomes are reported in three published analyses for sub-groups of the population.
Study assessing population-level CVD risk factors over a 6-year time frame before and
during project implementation (Sidebottom et al 2016)
Electronic health record data was used to assess changes in CVD risk factors for 7,855
people aged 40-79 at baseline (2008-09) and 2 follow-up periods (2010-11 and 2012-13).
Mean (standard deviation) age ranged from 56.4 (10.5) years at baseline to 57.6 (10.4) at
last follow-up and 53% were female.
The number of non-obese adults and the number achieving the high-density lipoprotein goal
did not significantly improve. The number of smokers increased from 11.3% to 13.6%. The
mean atherosclerotic (AS) CVD score improved but the number considered at low risk
(<7.5%) for a cardiovascular event did not significantly improve.
These results are also presented separately for men and women. Significant differences by
gender included greater increase in lipid use among women (improvement of 5.5% vs 1.8%
for men, p=0.001) and greater increase of men with fasting glucose at target (improvement
of 3.6% vs fluctuating scores for women, p=0.024). Women showed a significant
improvement in the proportion with an ASCVD score <7.5% (from 25.2% to 28.7%,
p=0.013). The corresponding improvement in men was not statistically significant.
Significant improvements in mean values for adults who had uncontrolled levels at baseline
were seen for blood pressure, low-density and high density lipoprotein, total cholesterol,
triglycerides, glucose and BMI. The proportion of this sub-group of adults who achieved
targets at follow-up was not reported.
The study authors reported that these improvements in the Heart of New Ulm population
were better than changes seen in national data over a similar time period.
Measures
Metabolic syndrome includes the presence of at least three of: abdominal obesity, high
blood pressure, low HDL cholesterol, high triglycerides and/or high blood glucose.
An Optimal Lifestyle Score was created with participants achieving 2 points (to a maximum
of 10 points) for optimal lifestyle thresholds. These were BMI <30kg/m2, being a non-
smoker, drinking <14 alcohol drinks per week, eating ≥5 servings fruit/vegetables per day
and ≥150 minutes per week of moderately equivalent physical activity. Difference
between2009 and 2011 OLS was classed as greatly improved (increase ≥4 points);
modestly improved (increased by 2 points); stayed the same (reference category);
decreased (decreased by ≥2 points).
Overall, adults lost 3.7% (± 11.2) of their work hours due to health reasons in 2011
(2009 figure not reported)
Significant association between smoking and productivity loss (9.3% for adults who
continued to smoke vs. 2.5% for adults who did not smoke during the 2 year period,
p=0.031)
No other lifestyle changes were significantly associated with workplace productivity loss
No figures reported for change from baseline for lifestyle measures
Change in lifestyle factors: Assessed using questions on smoking (never, current or former
smokers), alcohol use (drinks per week), fruit/vegetable consumption (servings per day) and
physical activity (minutes per week of moderately equivalent physical activity).
A Clinical Leadership team was formed to drive the health care objectives and included the
hospital president, local medical director, cardiologist medical director and physicians and
midlevel providers. This team met quarterly to discuss project initiatives.
Programmes were tailored to the local culture with the help of the steering committee and
informed by focus group and survey data from target audiences for specific programmes.
In order to ensure sustainability, part way through the funding period the researchers began
putting in place systems to support the continuation of the work across the community. A
main leadership group was formed with 11 sub-groups focused on progressing different
community approaches.
A leadership group of 12 key stakeholders strategically assess health needs and drive the
community priorities. The leadership team comprise representatives from schools, local
health services, large employers, chamber of commerce, local government, grocery stores
and food outlets. There are 11 action teams progressing the different community.
approaches.
Finances
Heart of New Ulm interventions were primarily funded by Allina Health, the health care
system operating the New Ulm Medical Center, with additional funding from government and
foundation grants.
The social marketing campaign ‘Swap It to Drop It’ was grant-funded. The ‘local health
system’ continued funding for dietician-led tours and the local grocery store hired a part-time
dietician.
In order to ensure sustainability, part way through the funding period the researchers began
putting in place systems to support the self-funding and continuation of the work across the
community.
At the end of the funding period when these externally funded roles disappeared, the
responsibility for these activities was integrated into the leadership team. The team is
formed of representatives working in a range of organisations across the community and
these organisations have committed a member of staff to be part of the team and the roles
and responsibilities are incorporated into their job descriptions.
The vast majority of the community get medical care from the New Ulm Medical Center,
which facilitated data tracking via electronic health records.
REFERENCES
Sidebottom AC. Sillah A. Miedema MD. Vock DM. Pereira R. Benson G. Boucher JL.
Knickelbine T. Lindberg R. VanWormer JJ. Changes in cardiovascular risk factors
after 5 years of implementation of a population-based program to reduce
cardiovascular disease: The Heart of New Ulm Project. American Heart Journal
2016, 175: 66-76
VanWormer JJ. Boucher JL. Sidebottom AC. Sillah A. Knickelbine T. Lifestyle
changes and prevention of metabolic syndrome in the Heart of New Ulm Project.
Preventative Medicine Reports 2017, 6: 242-245
VanWormer JJ. Boucher JL. Sidebottom AC. Two-year impact of lifestyle changes on
workplace productivity loss in the Heart of New Ulm Project. Occup. Environ Med
2015, 72: 460-462
A CASE STUDY
PROGRAMME AT A GLANCE
Hypertension Canada was formed in 2010 from the merger of
the Canadian Hypertension Society, the Canadian
Hypertension Education Program and Blood Pressure Canada.
Previously, all three organisations had worked independently to
improve hypertension diagnosis and management.
Hypertension Canada focusses on three main areas of activity:
Research - Building capacity and undertaking
hypertension surveillance
Education – Improvement of diagnosis and
management through dissemination of guidelines and KEY TAKEAWAYS
recommendations
Advocacy - Collaboration with stakeholders and Hypertension Canada
governments to create supportive environments through has worked to improve
improved awareness, prevention, and treatment the diagnosis and
control of hypertension
The main goal for Hypertension Canada is to ensure that across Canada
Canada continues to be effective in controlling hypertension
within the population. To do this Hypertension Canada is Canada controls
reducing misdiagnosis by ensuring that all healthcare hypertension in those
professionals in Canada are appropriately trained to diagnose
diagnosed with the
hypertension and follow recommended guidance to mange the condition better than
condition. most other countries.
Hypertension Canada is responsible for a number of the key
elements of hypertension control in Canada including: Hypertension Canada’s
work is based around
The production of annual evidence based guidelines on the creation of annually
hypertension treatment and management updated guidelines and
The establishment of a national healthcare public and recommendations
professional education programme
Encouraging the development of community Implementation of the
interventions and programmes guidelines is supported
Monitoring the progress of hypertension treatment and by an education
prevention initiatives in Canada. programme targeted at
In addition, Hypertension Canada and its predecessor health professionals
organisations have also worked with partners to achieve: and the public
PROGRAMME EXPERIENCES
Hypertension Canada uses a commercial
database to monitor trends in drug
prescriptions for people with hypertension,
allowing them to monitor increases in
antihypertensive medication prescriptions.
The coalition (which became known as Blood Pressure Canada) worked with the Canadian
Hypertension Society to develop a series of guidelines for assessing blood pressure (BP),
improving adherence to lifestyle and pharmacotherapy and home/self-assessment of blood
pressure. The coalition also developed a set of lifestyle recommendations that
systematically assessed and graded evidence and recommendations, as well as provided an
update to pharmacotherapy and diagnosis.
A refreshed national strategy was produced in the 1990’s led by Blood Pressure Canada. In
considering how to operationalise the strategy an enhanced guideline development process
was created, which became known as the Canadian Hypertension Education Program
(CHEP). Over time it became clear that help was needed to implement and evaluate the
impact of the CHEP guidelines and recommendations. This led to the creation of an
Implementation Task Force and subsequently an Outcomes Task Force.
In 2009, a process was developed that merged Blood Pressure Canada, CHEP, and the
Canadian Hypertension Society into a new organisation called Hypertension Canada that
has operated since 2010.
Hypertension Canada is a not for profit organisation committed to the prevention and control
of hypertension and its complications.
It cites its mission as being “Advancing health through the prevention and control of high
blood pressure and its complications” and has a vision that “Canadians will have the
healthiest and best managed blood pressure in the world”.
There are a number of key principles that govern how Hypertension Canada operates.
These include:
Evidence based - ensuring that all their work is evidence based, particularly in
relation to guideline development
Innovative – Hypertension Canada tries to encourage innovative practice, for
example in supporting single pill combination therapy, which avoids patients having
to take 3 – 4 different pills
Multi-disciplinary collaborative – the work of Hypertension Canada involves
professionals from many disciplines who collaborate to deliver the different elements
of Hypertension Canada’s work
Transparency – Hypertension Canada believes their work and guideline
development methodology should be transparent and open to challenge
Volunteer leadership – initially, the organisation was entirely volunteer-led, but now
there is a small number of paid staff in more managerial/director level roles.
Hypertension Canada strives to ensure that it engages healthcare professionals across all
disciplines to continually build credibility and relevance.
Population
Hypertension Canada’s work is aimed at all Canadians.
Service Delivery
Hypertension Canada use the diagram below to illustrate the key components of their work
programme.
The work being taken forward by Hypertension Canada to better prevent, diagnose and treat
hypertension in Canada is an ongoing effort.
The Taskforce has two co-chairs, a GP and a pharmacist. There are 16 sub-groups each
with a Chair and a small number of volunteer members and access to a librarian who does
all of the literature searching. The draft guidelines are reviewed and commented on by a
Central Review Committee which comprises experts in evidence based medicine and clinical
epidemiology. Once the Central Review Committee is happy with the draft guideline it goes
forward for presentation at an annual congress where all 81 members of the Taskforce vote
on whether to adopt the guideline or not, with 70% voting in favour being required for a
guideline to be adopted. After the Congress, a further round of on-line voting takes place, so
that any Taskforce members unable to attend the congress also get the chance to vote and
here a 75% majority is required for the guideline to be adopted.
Key messages from the Canadian Hypertension Education Program (CHEP) aimed a
healthcare professionals have included:
Hypertension Canada has succeeded in getting the importance of diagnosing and treating
hypertension included in the syllabus at a number of medical schools across the country.
Outcomes
Outcomes from Hypertension Canada’s work have been reported in published papers and in
a conference presentation and a webinar prepared for Public Health England.
A published paper detailing the history and development of Hypertension Canada (Shiffrin et
al, 2016) states that the Canadian Hypertension Education Program (CHEP) was associated
with increases in the proportion of diagnosed hypertension cases in Canada (from 57% in
1992 to 84.3% in 2013), the proportion of diagnosed cases receiving drug treatment (35% to
80%) and the control of hypertension (13% to 80%). It was also associated with large
reductions in the rates of death and hospitalisation from cardiovascular disease, acute
myocardial infarction, heart failure and stroke.
A published paper provided to SPH by Hypertension Canada (Padwal et al, 2016) about
the epidemiology of hypertension in Canada described a number of trends in aspects of
hypertension diagnosis and treatment.
The paper reported that the proportions of Canadians with hypertension detected and
treated had remained relatively stable since 2007-2009, but the proportion of
hypertension patients with controlled disease has increased from 65.9% in 2007-2009 to
68.1% in 2012/13 (Figure 2). The prevalence of hypertension was also found to have
increased from 19.6% to 22.6% over the same period.
Cycle 1 = 2007-2009
Cycle 2 = 2009-2011
Cycle 3 = 2012-2013
The paper also reported that in the diabetic population for the period 2012/13 the prevalence
of hypertension was 67.1% based on a threshold of 130/80 mm Hg. Of those with
hypertension 60.1% were treated and hypertension was controlled with a further 33.1% were
treated but hypertension was uncontrolled. If a threshold of 140/90 mm Hg was used for the
diagnosis of hypertension in respondents with diabetes, then 88.6% of respondents were
treated and the disease was controlled.
The paper noted that the number of antihypertensive prescriptions has increased steadily
since 2007, but prescribing costs have fallen, primarily due to cheaper generic medication
being available.
Figure 4: Trends in age-standardised mortality rates and relative risk ratio for those with and
without hypertension, 1998 - 2010
The October 2015 update to the 2011 Pan Canadian Hypertension Strategy written in 2015
detailed the progress made so far in achieving the various targets set within the 2011
strategy to be achieved by 2020. It suggested that based on the current trajectory, most of
the Framework targets are unlikely to be achieved by 2020. Based on survey data from the
Canadian Measurement Survey, there has been little change since 2011 in the prevalence of
hypertension, awareness of hypertension, diagnosis and control rates, suggesting that
preventative interventions have so far been less successful than interventions aimed at
those already diagnosed with hypertension.
Table 2: Progress towards 2020 targets set out in the 2011 Pan-Canadian hypertension
strategy
There is a small paid staff of 5 full time equivalent posts, with the majority of Hypertension
Canada’s work being delivered by volunteers on various committees, sub-groups and
taskforces.
Hypertension Canada’s guideline development process has been externally reviewed and
found to be in accordance with the Appraisal of Guidelines for Research and Education II
(AGREE II) instrument for guideline development.
Board of Directors
CEO Operations
Staff Committee
CHEP Standing
Recommendations Committees and
Task Force Task Forces
Finances
Hypertension Canada is a not for profit organisation and receives no government funding.
Funding is provided via sponsorships, from membership fees, from donations and from
sales. The latter relates to the Hypertension Canada’s Blood Pressure Measurement Device
Recommendation Program which allows manufacturers of blood pressure measurement
devices to submit their devices for validation by Hypertension Canada. Hypertension
Canada looks at the evidence base for the device and if it is in line with the evidence, the
manufacturer is allowed to use an approved by Hypertension Canada log in their
advertising/marketing material.
Human Resources
From 2000 to 2010 the number of people involved in the work now being taken forward by
Hypertension Canada increased from 20 to about 150.
The Hypertension Canada Research and Evaluation Committee (formerly the Outcomes
Research Taskforce) conducts surveillance studies on hypertension and reviews existing
Canadian health surveys to identify gaps between current and best practices.
Progress towards the targets included in the 2011 Pan Canadian Hypertension Framework
is monitored via the Canadian Measures Survey and by the Canadian Primary Care Sentinel
Surveillance Network.
REFERENCES
PHE Conference presentation on work of Hypertension Canada:
PHE Webinar on work of Hypertension Canada:
Campbell et al. A Framework for Discussion on How to Improve Prevention,
Management, and Control of Hypertension in Canada. Canadian Journal of
Cardiology 28 262–269. 2012.
Shiffrin et al. Hypertension in Canada: Past, Present and Future. Annals of Global
Health. Vol 82. No 2. 2016
Padwal et al. Epidemiology of Hypertension in Canada – An update. Canadian
Journal of Cardiology. 32 687-694. 2016
Nerenberg et al . Hypertension Canada’s 2018 Guidelines for Diagnosis, Risk
Assessment, Prevention, and Treatment of Hypertension in Adults and Children.
Canadian Journal of Cardiology 34 506e525. 2018
Hypertension Canada. Hypertension Prevention And Control In Canada: A Strategic
Approach To Save Lives, Improve Quality Of Life And Reduce Health Care Costs,
2015 Update
®
MILLION HEARTS INITIATIVE
A CASE STUDY
PROGRAMME AT A GLANCE
In 2012 the Million Hearts initiative was established by the
US Department of Health and Human Services, the Centre
for Disease Control and Prevention (CDC) and Centres for
Medicare and Medicaid (CMS). This national initiative had a
first phase, 5-year goal, of preventing 1 million
cardiovascular events by 2017, and is now in its second
phase, Million Hearts 2022.
Million Hearts works to align CVD prevention efforts across KEY TAKE AWAYS
50 states and 120 partners in the US by focussing on a small
set of evidence-based priorities selected for their impact on The public, private and
heart disease, stroke and related conditions. non-profit sectors have
Promoting clinical quality improvement such as the been encouraged to
implementation of the ABCS approach to CVD management work together in a
(Aspirin when appropriate, Blood pressure control, coordinated way to
Cholesterol management, and Smoking cessation) and achieve targets and
meaningful use of health tools and technology such as share goals.
electronic records for identifying and monitoring patient
groups are key activities. Community approaches include The aim to prevent a
introducing policies to eliminate artificial trans-fat intake, million CVD events was
reduce tobacco use and reduce sodium intake. easily understood and
resonated with diverse
Million Hearts 2022 continues these activities but new stakeholders. Focus
emphasis is placed on achieving 70% participation in cardiac on a limited set of
rehabilitation by 2022. Key to achieving these aims are: proven, high-impact
Health care teams prioritise detection, treatment and interventions helped
control and review data regularly to keep on track partners prioritise their
Using technology that includes decision support, efforts.
patient portals, registries, and algorithms to find gaps
in care Million Hearts has been
Processes around treatment protocols, proactive integrated into nursing
outreach and finding patients with undiagnosed high and inter-professional
BP, cholesterol or tobacco use educational curricula
Patient and Family Supports – training in home BP and community settings
monitoring, problem solving in medication adherence,
counselling on nutrition, physical activity, tobacco
use, referral to community-based physical activity
programs and cardiac rehabilitation
Health care professionals and health care
organisations promote activities that reduce the
likelihood of CVD such as increased physical activity,
healthy eating and smoking cessation.
TARGET POPULATION incentive programs rewarded health
care practices for achieving
In its first phase, of Million Hearts the
meaningful use of EHRs. Use of
programme targeted the US population to
EHRs for outpatient care increased
support activities and policies to develop
from 34% in 2011 to 87% in 2015.
healthier habits and environments for
Health information technology has
people in all communities. The second
helped identify more than half a
phase Million Hearts 2022 continues to
million people who may have
develop effective public health strategies
hypertension.
but also identified priority populations
including African Americans, 35-64 year Innovations in Care Delivery: Health
olds, people who have had a heart attack care systems have been able to
or stroke and people with mental and/or use millions of dollars in public and
substance use disorders. private funds to improve
performance on the ABCS.
BENEFITS AND OUTCOMES
During the first two years of the initiative, it PROGRAMME EXPERIENCES
is estimated that about 115,000
cardiovascular events were prevented, The strength of the network and its
relative to the number of events in 2011 partnerships are viewed as key to
and 500,000 between 2012 and 2016. the success of Million Hearts.
These events include emergency Organisations apply to be partners
department visits, hospitalizations, and through the Million Hearts website
deaths due to myocardial infarction, stroke, and a range of resources are
heart failure, and related conditions. available providing platforms of
However final numbers will not be available communication and shared
until 2019. The reduction in events cannot learning.
be attributed solely to the initiative, but the The first phase Million Hearts 2017
reduction is noteworthy because, until informed the strategy of Million
2011, there had been a flattening trend in Hearts 2022, identifying priority
CVD mortality. Outcomes include: populations and additional areas of
focus such as cardiac rehabilitation.
ABCS measures were widely There was delayed federal action
adopted with an on overall on guidance to the food industry for
controlled hypertension rate for the voluntarily reduction in sodium in
US of 58% in 2016 up from 53% in processed and commercially
2009/10 prepared food was issued in June
Controlled hypertension was 2016 which slowed progress.
reported in 80% of hypertensives by There was delayed federal action
59 hypertension control champions on announcing that partially
covering 13.8 million people hydrogenated oils were not safe so.
Reduction in smoking: 7 million Policy in place during 2018.
fewer people smoked cigarettes in Key indicators have been slow to
2015 than in 2011. improve but it is hoped that with a
Increase of 48.1% to 58.8% raft of guidance, training policies
between 2011 and 2016 of and initiatives now in place there
population covered with will be an acceleration of progress.
comprehensive smoke free law
Millions of Americans are now
served by health care systems that
recognise or reward performance in
the ABCS e.g. the Million Hearts
Hypertension Control Challenge
Health Tools and Technology: CMS
Electronic Health Record (EHR)
THE DETAIL
Context
Million Hearts supports community activities and policies that it is hoped will result in
healthier habits and environments for people across the US, such as reducing smoking,
reducing sodium intake and eliminating trans-fat intake. It also focuses on clinical quality
improvements related to ABCS measures(Aspirin when appropriate, Blood pressure control,
Cholesterol management, and Smoking cessation), use of health tools and technology to
detect CVD risk and innovations in care delivery. The engagement of partners and ongoing
collaboration was a key and clear aim of preventing a million events, a message easily
understood by stakeholders. Some interventions are implemented at national level affecting
the whole population, for example, policy change on trans-fats and guidance on sodium
reduction, and others, such as meeting the ABCS, are enacted at local level and are
targeted at those identified as having specific high risk factors.
Million Hearts 2022 continues these activities but new emphasis is placed on achieving 70%
participation in cardiac rehabilitation by 2022, and priority populations have been identified.
The program is challenging the clinical health system and the public health community to
increase their collaboration to prevent cardiovascular disease by focusing on the ABCS,
increasing use of health information technology including electronic health records, and
integrating team-based care into everyday practice. Public health helps clinical care by
making the case for effective public policies such as reducing salt and trans-fat in prepared
foods and establishing smoke-free environments to help prevent heart attacks and strokes.
Working with communities, health systems, non-profit organisations, federal agencies, and
private sector partners, the collaborative approach is an important feature of the initiative.
Varda et al (2018) used a social network analysis approach to assess the Million Hearts
network partnerships and identify potential implications for policy and practice. The authors
conclude that the Million Hearts network is unique in its membership at the national level,
agreement on outcomes and information-sharing abilities that require few resources. There
is a decentralized structure with the core team and stakeholders continuing to find ways to
strengthen the network.
Frieden et al (2017) note that the programmes aim to prevent a million events was easily
understood and resonated with diverse stakeholders, as did the concept of public health and
health care working together toward a common goal. The five year time frame gave a sense
of urgency and focusing on a limited set of proven, high-impact interventions helped partners
prioritize their efforts. Flexibility implementing interventions made diverse participation
possible.
Million Hearts supports individuals and organisations that are currently or aiming to put
resource into CVD prevention and encourage them to focus on implementing the ABCS and
other evidence based interventions that are likely to make a difference. “Waste no will” is a
key principle which leads to inclusivity of all organisations that have the goal of reducing the
risk factors that lead to CVD. This inclusivity results in diverse partners networking with each
other who may not otherwise have met.
Ades et al (2016) outline a ‘road map’ to achieving 70% participation in cardiac rehabilitation
and secondary prevention programs by the year 2022. Current participation rates for cardiac
rehabilitation in the United States generally range from only 20% to 30%. The road map
focuses on interventions, such as electronic medical record–based prompts and staffing
liaisons that increase referrals of appropriate patients to cardiac rehabilitation services and
adherence to cardiac rehabilitation programmes. The authors calculate that increasing
cardiac rehabilitation participation from 20% to 70% would save 25,000 lives and prevent
180,000 hospitalizations annually in the United States.
Population
The Million Hearts program covers the whole of the US and the initial goal was to prevent a
million CVD events nationally, between 2012 and 2017.
Service Delivery
The Million Hearts small core team is based in CDC where they:
Organisations can apply for funding from Million Hearts for short term projects to implement
an initiative that the organisation will sustain after this time. This funding is for innovative
projects that further the specific objectives of Million Hearts which include:
encouraging health care teams to prioritise detection, treatment and control and
review data regularly to keep on track
using technology that includes decision support, patient portals, registries, and
algorithms to find gaps in care
processes around treatment protocols and the ABCS, proactive outreach and finding
patients with undiagnosed high BP, cholesterol or tobacco use
patient and family supports – training in home BP monitoring, problem solving in
medication adherence, counselling on nutrition, physical activity, tobacco use,
referral to community-based physical activity programs and cardiac rehabilitation.
Partner organisations vary in size (from individual practices to large corporate organisations)
and health focus (from prevention to cardiac rehabilitation) so will deliver services differently
and on different scales.
The public, private and non-profit health sectors were encouraged to work together in a
coordinated way to achieve these targets and share goals.
In addition Million Hearts has been integrated into nursing and inter-professional educational
curricula and community settings (Gawlik et al 2015). The National Inter-professional
Education and Practice Consortium to Advance Million Hearts was created, and a free on-
line educational module was developed to help health care professionals and students learn
about the Million Hearts initiative, conduct community CVD risk factor screening, and refer
people who screen positive to appropriate resources. After completion of the module,
individuals receive certification as a Million Hearts Fellow. The module and CVD risk factor
screening has been incorporated into health sciences curricula. Academic institutions and
health science professions partnering together as part of the National Inter-professional
Education and Practice Consortium to Advance Million Hearts provide a unique opportunity
to demonstrate the impact that a unified approach can have on improving population health
through the use of screening, education, and prevention.
Primary prevention
Reduction in smoking: 7 million fewer people smoked cigarettes in 2015 than in 2011.
Reduction in sodium intake: Draft guidance to the food industry for voluntarily reducing
sodium in processed and commercially prepared food was issued in June 2016. This step
was intended to help Americans gradually reduce their sodium intake to the recommended
level of less than 2,300 mg per day, which will improve their blood pressure
Eliminate trans-fat intake: Partially hydrogenated oils were expected to be removed from the
food supply by 2018 with the intention of preventing thousands of fatal heart attacks every
year. Legislation passed in June 2015 required that within three years, all food prepared in
the US must not include trans-fats, unless approved by the Food and Drug Administration
(FDA). In May 2018 the FDA agreed to give companies one more year to find an alternative
ingredient.
ABCS clinical quality measures have been embedded in national reporting and performance
programs and performance in the ABCS has been rewarded e.g. the Million Hearts
A focus on the ABCS has generated slow but steady improvement nationally in aspirin use,
blood pressure control, and statin use among people who are eligible based on current
guidelines. There is some variability in compliance with the ABCS quality measures and
there are opportunities for improvement (Eapen et al 2014).
Young et al (2018) identified characteristics of health care practices and systems effective in
achieving control rates at or above 70% by using data collected via applications submitted
from April through June 2017 for consideration in the Million Hearts Hypertension Control
Challenge.
They included 96 practices serving 635,000 patients with hypertension across 34 US states
in the analysis. Mean hypertension control rate was 77.1% with 27.1% of practices having a
control rate of 80% or greater. Although many practices served large populations with
multiple risk factors for uncontrolled hypertension, high control rates were achieved with
implementation of multiple evidenced-based strategies.
There were some factors common to these practices including:
Using multiple strategies to achieve high BP control rates aligned with the World
Health Organization’s Innovative Care for Chronic Conditions recommendations, and
strategies recommended by the Centers for Disease Control and Prevention funded
State Public Health Actions grantees and Million Hearts.
Having electronic health records with features such as electronic prescribing, patient
registries, and clinical decision support tools
Implementing hypertension treatment protocols. This helps standardize and
coordinate care and facilities a team approach to BP management
Some practices were offered financial and other incentives to clinicians and patients
to encourage greater attention to BP control by health insurers
Engaging patients in BP home monitoring to assess progress, inform decision
making, and encourage adherence to treatment regimens
Freidan et al (2017) >125,000 physicians who were part of the electronic health records
Medicare incentive programme reported an average blood pressure control rate of 62%
across >17 million people with hypertension.
Cholesterol Management
In 2013, the American College of Cardiology (ACC) and the American Heart
Association (AHA) released new clinical guidelines on the treatment of blood
cholesterol to reduce atherosclerotic CVD (ASCVD) risk in adults.
The new guidelines focus only on statin use in (1) adults with clinical ASCVD, (2)
adults with LDL ≥190 mg/ dL, (3) adults aged 40–75 years with type 1 or 2 diabetes,
and (4) adults aged 40–75 years with an estimated 10-year ASCVD risk of at least
7.5%.
A federal workgroup drafted a new “Statin Therapy for the Prevention and Treatment
of Cardiovascular Disease” measure. This measure assesses statin use among the
first three of the four risk groups (see above bullet point) and will be available during
2018 for electronic health record reporting.
Retrospective analysis reflecting statin use among all four groups of eligible people,
using 2005–2012 NHANES data, show that statin use has been steadily on the rise
since at least 2005–2006 (see Figure 2).
Health Tools and Technology: Electronic Health Record (EHR) Incentive Programs
rewarded health care practices for achieving meaningful use of EHRs. Use of EHRs for
outpatient care increased from 34% in 2011 to 87% in 2015. Health information technology
has helped identify more than half a million people who may have hypertension.
Organizations can apply to be partners through the Million Hearts website and a range of
resources are available providing platforms of communication and shared learning. The
Million Hearts network is comprised of a core group of federal and private sector partners
that regularly participate in Million Hearts activities.
Varda et al (2018) conducted a social network analysis. This too analysed how partners are
connected, how resources are exchanged, the levels of trust and perceived value among
The perceptions between partners are that resources are not being contributed at the level
they potentially could be. The majority of partners reported that being in the network helped
them achieve their goals related to cardiovascular disease prevention. The largest barrier to
successful activities within the network was cited as lack of targeted funding and staff to
support participation in the network. However the network is unique in its membership at the
national level, agreement on outcomes, information-sharing abilities that require few
resources. It has a decentralized structure, with a core team identifying ways to strengthen
the network.
Finances
The core team, funded through CDC that works to distribute funding and support networks of
partners, and information gathering.
Organisations can apply for funding from Million Hearts for short term projects to implement
an initiative that the organisation will sustain after this time. This funding tends to be for
innovative projects such as helping health centres use their clinical data to identify potentially
hypertensive patients, or work to improve numbers of people monitoring their own blood
pressure.
Partners join the network because they have a common aim to reduce the risk of CVD and
take part in challenges, apply for funding, receive incentives from medical insurers or
voluntarily develop services to meet the Million Hearts goals.
Human Resources
The core team comprise:
Population level surveys are utilised, and though accurate may not be timely for the
purposes of Million Hearts. The Million Hearts team tend to ‘amass data patches’ from
health systems and local data in order to build a national picture. There are national
surveillance data systems that are pieced together for various intermediate and long term
indicators. There is a small set of clinical indicators that Million Hearts have worked to
On occasion a clinic or local health system may look at their data and choose to share it with
Million Hearts and this is encouraged by, for example, the Champion Program for blood
pressure.
Often spontaneous regional public health/health care collaborations arise using the Million
Hearts framework. There is confidence in using framework developed by an independent
government agency and there is flexibility about what to implement for their particular
population.
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